Canonical Allele Identifier: CA1053029916
Gene: MYLK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123689532_123689538del , CM000665.2:g.123689532_123689538del GRCh38
NC_000003.11:g.123408379_123408385del , CM000665.1:g.123408379_123408385del GRCh37
NC_000003.10:g.124891069_124891075del NCBI36
NG_029111.1:g.199765_199771del

Transcript Alleles

HGVS Amino-acid Change
ENST00000346322.10:c.3358+3197_3358+3203del ENSP00000320622.6:n.3358+3197_3358+3203del
ENST00000504946.6:c.1175+3197_1175+3203del
ENST00000508240.2:c.-36+2745_-36+2751del ENSP00000422984.2:n.-36+2745_-36+2751del
ENST00000684879.1:n.1197+3197_1197+3203del
ENST00000685021.1:c.799+3197_799+3203del ENSP00000508447.1:n.799+3197_799+3203del
ENST00000685259.1:c.1103+3197_1103+3203del
ENST00000685907.1:n.1346+3197_1346+3203del
ENST00000685953.1:c.-36+2745_-36+2751del ENSP00000510593.1:n.-36+2745_-36+2751del
ENST00000686039.1:c.1103+3197_1103+3203del
ENST00000686245.1:c.683-7228_683-7222del ENSP00000509313.1:n.683-7228_683-7222del
ENST00000686406.1:c.3565+3197_3565+3203del ENSP00000509044.1:n.3565+3197_3565+3203del
ENST00000686761.1:c.3565+3197_3565+3203del ENSP00000508758.1:n.3565+3197_3565+3203del
ENST00000686822.1:n.3459+3197_3459+3203del
ENST00000687434.1:c.-36+2745_-36+2751del ENSP00000509751.1:n.-36+2745_-36+2751del
ENST00000687709.1:n.830+3197_830+3203del
ENST00000687848.1:c.3595+3197_3595+3203del ENSP00000508761.1:n.3595+3197_3595+3203del
ENST00000688024.1:c.799+3197_799+3203del ENSP00000509803.1:n.799+3197_799+3203del
ENST00000688223.1:c.799+3197_799+3203del ENSP00000508935.1:n.799+3197_799+3203del
ENST00000689227.1:c.1238+3197_1238+3203del
ENST00000689868.1:n.1293+3197_1293+3203del
ENST00000690167.1:n.1236+3197_1236+3203del
ENST00000690457.1:c.2803+3197_2803+3203del ENSP00000508777.1:n.2803+3197_2803+3203del
ENST00000691933.1:c.1103+3197_1103+3203del
ENST00000692352.1:c.1103+3197_1103+3203del
ENST00000693689.1:c.3358+3197_3358+3203del ENSP00000510503.1:n.3358+3197_3358+3203del
ENST00000360304.8:c.3565+3197_3565+3203del MANE Select ENSP00000353452.3:n.3565+3197_3565+3203del
ENST00000346322.9:c.3358+3197_3358+3203del ENSP00000320622.5:n.3358+3197_3358+3203del
ENST00000354792.9:c.3358+3197_3358+3203del ENSP00000346846.6:n.3358+3197_3358+3203del
ENST00000359169.5:c.3565+3197_3565+3203del ENSP00000352088.1:n.3565+3197_3565+3203del
ENST00000360304.7:c.3565+3197_3565+3203del ENSP00000353452.3:n.3565+3197_3565+3203del
ENST00000360772.7:c.3565+3197_3565+3203del ENSP00000354004.3:n.3565+3197_3565+3203del
ENST00000464489.5:c.*3144+3197_*3144+3203del ENSP00000417798.1:n.*3144+3197_*3144+3203del
ENST00000475616.5:c.3565+3197_3565+3203del ENSP00000418335.1:n.3565+3197_3565+3203del
ENST00000504946.5:n.1123+3197_1123+3203del
ENST00000508240.1:c.-36+2745_-36+2751del ENSP00000422984.1:n.-36+2745_-36+2751del
ENST00000510775.5:n.283+3197_283+3203del
NM_053025.3:c.3565+3197_3565+3203del NP_444253.3:n.3565+3197_3565+3203del
NM_053026.3:c.3358+3197_3358+3203del NP_444254.3:n.3358+3197_3358+3203del
NM_053027.3:c.3565+3197_3565+3203del NP_444255.3:n.3565+3197_3565+3203del
NM_053028.3:c.3358+3197_3358+3203del NP_444256.3:n.3358+3197_3358+3203del
XM_011512860.1:c.3565+3197_3565+3203del XP_011511162.1:n.3565+3197_3565+3203del
XM_011512861.1:c.3565+3197_3565+3203del XP_011511163.1:n.3565+3197_3565+3203del
XM_011512862.1:c.3037+3197_3037+3203del XP_011511164.1:n.3037+3197_3037+3203del
NM_001321309.1:c.3037+3197_3037+3203del NP_001308238.1:n.3037+3197_3037+3203del
XM_011512860.3:c.3595+3197_3595+3203del XP_011511162.2:n.3595+3197_3595+3203del
XM_011512861.3:c.3595+3197_3595+3203del XP_011511163.2:n.3595+3197_3595+3203del
XM_017006469.2:c.799+3197_799+3203del XP_016861958.1:n.799+3197_799+3203del
XM_017006470.2:c.-36+2745_-36+2751del XP_016861959.1:n.-36+2745_-36+2751del
XM_017006471.2:c.-36+2745_-36+2751del XP_016861960.1:n.-36+2745_-36+2751del
XM_024453532.1:c.3595+3197_3595+3203del XP_024309300.1:n.3595+3197_3595+3203del
XM_024453533.1:c.3565+3197_3565+3203del XP_024309301.1:n.3565+3197_3565+3203del
XM_024453534.1:c.3388+3197_3388+3203del XP_024309302.1:n.3388+3197_3388+3203del
XM_024453535.1:c.3358+3197_3358+3203del XP_024309303.1:n.3358+3197_3358+3203del
XM_024453536.1:c.3565+3197_3565+3203del XP_024309304.1:n.3565+3197_3565+3203del
XM_024453537.1:c.3565+3197_3565+3203del XP_024309305.1:n.3565+3197_3565+3203del
NM_001321309.2:c.3037+3197_3037+3203del NP_001308238.1:n.3037+3197_3037+3203del
NM_053025.4:c.3565+3197_3565+3203del MANE Select NP_444253.3:n.3565+3197_3565+3203del
NM_053026.4:c.3358+3197_3358+3203del NP_444254.3:n.3358+3197_3358+3203del
NM_053027.4:c.3565+3197_3565+3203del NP_444255.3:n.3565+3197_3565+3203del
NM_053028.4:c.3358+3197_3358+3203del NP_444256.3:n.3358+3197_3358+3203del