Canonical Allele Identifier: CA2667295219

Gene: MYLK

Linked Data

• gnomAD v4: 3-123692721-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123692723_123692724del , CM000665.2:g.123692723_123692724del	GRCh38
NC_000003.11:g.123411570_123411571del , CM000665.1:g.123411570_123411571del	GRCh37
NC_000003.10:g.124894260_124894261del	NCBI36
NG_029111.1:g.196580_196581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.3358+12_3358+13del	ENSP00000320622.6:n.3358+12_3358+13del
ENST00000504946.6:c.1175+12_1175+13del
ENST00000684879.1:n.1197+12_1197+13del
ENST00000685021.1:c.799+12_799+13del	ENSP00000508447.1:n.799+12_799+13del
ENST00000685259.1:c.1103+12_1103+13del
ENST00000685907.1:n.1346+12_1346+13del
ENST00000686039.1:c.1103+12_1103+13del
ENST00000686245.1:c.682+7297_682+7298del	ENSP00000509313.1:n.682+7297_682+7298del
ENST00000686406.1:c.3565+12_3565+13del	ENSP00000509044.1:n.3565+12_3565+13del
ENST00000686761.1:c.3565+12_3565+13del	ENSP00000508758.1:n.3565+12_3565+13del
ENST00000686822.1:n.3459+12_3459+13del
ENST00000687709.1:n.830+12_830+13del
ENST00000687848.1:c.3595+12_3595+13del	ENSP00000508761.1:n.3595+12_3595+13del
ENST00000688024.1:c.799+12_799+13del	ENSP00000509803.1:n.799+12_799+13del
ENST00000688223.1:c.799+12_799+13del	ENSP00000508935.1:n.799+12_799+13del
ENST00000689227.1:c.1238+12_1238+13del
ENST00000689868.1:n.1293+12_1293+13del
ENST00000690167.1:n.1236+12_1236+13del
ENST00000690457.1:c.2803+12_2803+13del	ENSP00000508777.1:n.2803+12_2803+13del
ENST00000691933.1:c.1103+12_1103+13del
ENST00000692352.1:c.1103+12_1103+13del
ENST00000693689.1:c.3358+12_3358+13del	ENSP00000510503.1:n.3358+12_3358+13del
ENST00000360304.8:c.3565+12_3565+13del MANE Select	ENSP00000353452.3:n.3565+12_3565+13del
ENST00000346322.9:c.3358+12_3358+13del	ENSP00000320622.5:n.3358+12_3358+13del
ENST00000354792.9:c.3358+12_3358+13del	ENSP00000346846.6:n.3358+12_3358+13del
ENST00000359169.5:c.3565+12_3565+13del	ENSP00000352088.1:n.3565+12_3565+13del
ENST00000360304.7:c.3565+12_3565+13del	ENSP00000353452.3:n.3565+12_3565+13del
ENST00000360772.7:c.3565+12_3565+13del	ENSP00000354004.3:n.3565+12_3565+13del
ENST00000464489.5:c.*3144+12_*3144+13del	ENSP00000417798.1:n.*3144+12_*3144+13del
ENST00000475616.5:c.3565+12_3565+13del	ENSP00000418335.1:n.3565+12_3565+13del
ENST00000504946.5:n.1123+12_1123+13del
ENST00000510775.5:n.283+12_283+13del
NM_053025.3:c.3565+12_3565+13del	NP_444253.3:n.3565+12_3565+13del
NM_053026.3:c.3358+12_3358+13del	NP_444254.3:n.3358+12_3358+13del
NM_053027.3:c.3565+12_3565+13del	NP_444255.3:n.3565+12_3565+13del
NM_053028.3:c.3358+12_3358+13del	NP_444256.3:n.3358+12_3358+13del
XM_011512860.1:c.3565+12_3565+13del	XP_011511162.1:n.3565+12_3565+13del
XM_011512861.1:c.3565+12_3565+13del	XP_011511163.1:n.3565+12_3565+13del
XM_011512862.1:c.3037+12_3037+13del	XP_011511164.1:n.3037+12_3037+13del
NM_001321309.1:c.3037+12_3037+13del	NP_001308238.1:n.3037+12_3037+13del
XM_011512860.3:c.3595+12_3595+13del	XP_011511162.2:n.3595+12_3595+13del
XM_011512861.3:c.3595+12_3595+13del	XP_011511163.2:n.3595+12_3595+13del
XM_017006469.2:c.799+12_799+13del	XP_016861958.1:n.799+12_799+13del
XM_024453532.1:c.3595+12_3595+13del	XP_024309300.1:n.3595+12_3595+13del
XM_024453533.1:c.3565+12_3565+13del	XP_024309301.1:n.3565+12_3565+13del
XM_024453534.1:c.3388+12_3388+13del	XP_024309302.1:n.3388+12_3388+13del
XM_024453535.1:c.3358+12_3358+13del	XP_024309303.1:n.3358+12_3358+13del
XM_024453536.1:c.3565+12_3565+13del	XP_024309304.1:n.3565+12_3565+13del
XM_024453537.1:c.3565+12_3565+13del	XP_024309305.1:n.3565+12_3565+13del
NM_001321309.2:c.3037+12_3037+13del	NP_001308238.1:n.3037+12_3037+13del
NM_053025.4:c.3565+12_3565+13del MANE Select	NP_444253.3:n.3565+12_3565+13del
NM_053026.4:c.3358+12_3358+13del	NP_444254.3:n.3358+12_3358+13del
NM_053027.4:c.3565+12_3565+13del	NP_444255.3:n.3565+12_3565+13del
NM_053028.4:c.3358+12_3358+13del	NP_444256.3:n.3358+12_3358+13del