Canonical Allele Identifier: CA1398493211
Gene: MYLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123647469A= , CM000665.2:g.123647469A= GRCh38
NC_000003.11:g.123366316A= , CM000665.1:g.123366316A= GRCh37
NC_000003.10:g.124849006A= NCBI36
NG_029111.1:g.241834T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000346322.10:c.4209-42T= ENSP00000320622.6:n.4209-42T=
ENST00000508240.2:c.816-42T= ENSP00000422984.2:n.816-42T=
ENST00000513111.2:n.546-42T=
ENST00000684879.1:n.2048-42T=
ENST00000685021.1:c.1650-42T= ENSP00000508447.1:n.1650-42T=
ENST00000685259.1:c.1935-42T=
ENST00000685907.1:n.2197-42T=
ENST00000685953.1:c.816-42T= ENSP00000510593.1:n.816-42T=
ENST00000686039.1:c.1800-42T=
ENST00000686245.1:c.1533-42T= ENSP00000509313.1:n.1533-42T=
ENST00000686406.1:c.4416-42T= ENSP00000509044.1:n.4416-42T=
ENST00000686458.1:n.918-42T=
ENST00000686761.1:c.4416-42T= ENSP00000508758.1:n.4416-42T=
ENST00000686822.1:n.4310-42T=
ENST00000687434.1:c.*632-42T= ENSP00000509751.1:n.*632-42T=
ENST00000687709.1:n.2471-42T=
ENST00000687848.1:c.4446-42T= ENSP00000508761.1:n.4446-42T=
ENST00000688024.1:c.1650-42T= ENSP00000509803.1:n.1650-42T=
ENST00000688223.1:c.1649+1502T= ENSP00000508935.1:n.1649+1502T=
ENST00000689868.1:n.2144-42T=
ENST00000689918.1:n.491-42T=
ENST00000690086.1:n.517-42T=
ENST00000690167.1:n.2087-42T=
ENST00000690457.1:c.3654-42T= ENSP00000508777.1:n.3654-42T=
ENST00000690534.1:n.937-42T=
ENST00000691933.1:c.2040-42T=
ENST00000692352.1:c.1954-42T=
ENST00000693689.1:c.4209-42T= ENSP00000510503.1:n.4209-42T=
ENST00000360304.8:c.4416-42T= MANE Select ENSP00000353452.3:n.4416-42T=
ENST00000346322.9:c.4209-42T= ENSP00000320622.5:n.4209-42T=
ENST00000354792.9:c.4209-42T= ENSP00000346846.6:n.4209-42T=
ENST00000359169.5:c.4416-42T= ENSP00000352088.1:n.4416-42T=
ENST00000360304.7:c.4416-42T= ENSP00000353452.3:n.4416-42T=
ENST00000360772.7:c.4416-42T= ENSP00000354004.3:n.4416-42T=
ENST00000464489.5:c.*3995-42T= ENSP00000417798.1:n.*3995-42T=
ENST00000475616.5:c.4416-42T= ENSP00000418335.1:n.4416-42T=
ENST00000513111.1:n.128-42T=
ENST00000514895.5:n.94+1502T=
NM_053025.3:c.4416-42T= NP_444253.3:n.4416-42T=
NM_053026.3:c.4209-42T= NP_444254.3:n.4209-42T=
NM_053027.3:c.4416-42T= NP_444255.3:n.4416-42T=
NM_053028.3:c.4209-42T= NP_444256.3:n.4209-42T=
XM_011512860.1:c.4416-42T= XP_011511162.1:n.4416-42T=
XM_011512861.1:c.4415+1502T= XP_011511163.1:n.4415+1502T=
XM_011512862.1:c.3888-42T= XP_011511164.1:n.3888-42T=
NM_001321309.1:c.3888-42T= NP_001308238.1:n.3888-42T=
XM_011512860.3:c.4446-42T= XP_011511162.2:n.4446-42T=
XM_011512861.3:c.4445+1502T= XP_011511163.2:n.4445+1502T=
XM_017006469.2:c.1650-42T= XP_016861958.1:n.1650-42T=
XM_017006470.2:c.816-42T= XP_016861959.1:n.816-42T=
XM_017006471.2:c.816-42T= XP_016861960.1:n.816-42T=
XM_024453532.1:c.4446-42T= XP_024309300.1:n.4446-42T=
XM_024453533.1:c.4416-42T= XP_024309301.1:n.4416-42T=
XM_024453534.1:c.4239-42T= XP_024309302.1:n.4239-42T=
XM_024453535.1:c.4209-42T= XP_024309303.1:n.4209-42T=
XM_024453536.1:c.4416-42T= XP_024309304.1:n.4416-42T=
XM_024453537.1:c.4416-42T= XP_024309305.1:n.4416-42T=
NM_001321309.2:c.3888-42T= NP_001308238.1:n.3888-42T=
NM_053025.4:c.4416-42T= MANE Select NP_444253.3:n.4416-42T=
NM_053026.4:c.4209-42T= NP_444254.3:n.4209-42T=
NM_053027.4:c.4416-42T= NP_444255.3:n.4416-42T=
NM_053028.4:c.4209-42T= NP_444256.3:n.4209-42T=