Canonical Allele Identifier: CA1398493133
Gene: MYLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123647265A= , CM000665.2:g.123647265A= GRCh38
NC_000003.11:g.123366112A= , CM000665.1:g.123366112A= GRCh37
NC_000003.10:g.124848802A= NCBI36
NG_029111.1:g.242038T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000346322.10:c.4371T= ENSP00000320622.6:p.Asp1457=
ENST00000508240.2:c.978T= ENSP00000422984.2:p.Asp326=
ENST00000513111.2:n.708T=
ENST00000684879.1:n.2210T=
ENST00000685021.1:c.1812T= ENSP00000508447.1:p.Asp604=
ENST00000685259.1:c.2097T=
ENST00000685907.1:n.2359T=
ENST00000685953.1:c.978T= ENSP00000510593.1:p.Asp326=
ENST00000686039.1:c.1962T=
ENST00000686245.1:c.1695T= ENSP00000509313.1:p.Asp565=
ENST00000686406.1:c.4578T= ENSP00000509044.1:p.Asp1526=
ENST00000686458.1:n.1080T=
ENST00000686761.1:c.4578T= ENSP00000508758.1:p.Asp1526=
ENST00000686822.1:n.4472T=
ENST00000687434.1:c.*794T= ENSP00000509751.1:n.*794T=
ENST00000687709.1:n.2633T=
ENST00000687848.1:c.4608T= ENSP00000508761.1:p.Asp1536=
ENST00000688024.1:c.1812T= ENSP00000509803.1:p.Asp604=
ENST00000688223.1:c.1649+1706T= ENSP00000508935.1:n.1649+1706T=
ENST00000689868.1:n.2306T=
ENST00000689918.1:n.653T=
ENST00000690086.1:n.679T=
ENST00000690167.1:n.2249T=
ENST00000690457.1:c.3816T= ENSP00000508777.1:p.Asp1272=
ENST00000690534.1:n.1099T=
ENST00000691933.1:c.2202T=
ENST00000692352.1:c.2116T=
ENST00000693689.1:c.4371T= ENSP00000510503.1:p.Asp1457=
ENST00000360304.8:c.4578T= MANE Select ENSP00000353452.3:p.Asp1526=
ENST00000346322.9:c.4371T= ENSP00000320622.5:p.Asp1457=
ENST00000354792.9:c.4371T= ENSP00000346846.6:p.Asp1457=
ENST00000359169.5:c.4578T= ENSP00000352088.1:p.Asp1526=
ENST00000360304.7:c.4578T= ENSP00000353452.3:p.Asp1526=
ENST00000360772.7:c.4578T= ENSP00000354004.3:p.Asp1526=
ENST00000464489.5:c.*4157T= ENSP00000417798.1:n.*4157T=
ENST00000475616.5:c.4578T= ENSP00000418335.1:p.Asp1526=
ENST00000513111.1:n.290T=
ENST00000514895.5:n.94+1706T=
NM_053025.3:c.4578T= NP_444253.3:p.Asp1526=
NM_053026.3:c.4371T= NP_444254.3:p.Asp1457=
NM_053027.3:c.4578T= NP_444255.3:p.Asp1526=
NM_053028.3:c.4371T= NP_444256.3:p.Asp1457=
XM_011512860.1:c.4578T= XP_011511162.1:p.Asp1526=
XM_011512861.1:c.4415+1706T= XP_011511163.1:n.4415+1706T=
XM_011512862.1:c.4050T= XP_011511164.1:p.Asp1350=
NM_001321309.1:c.4050T= NP_001308238.1:p.Asp1350=
XM_011512860.3:c.4608T= XP_011511162.2:p.Asp1536=
XM_011512861.3:c.4445+1706T= XP_011511163.2:n.4445+1706T=
XM_017006469.2:c.1812T= XP_016861958.1:p.Asp604=
XM_017006470.2:c.978T= XP_016861959.1:p.Asp326=
XM_017006471.2:c.978T= XP_016861960.1:p.Asp326=
XM_024453532.1:c.4608T= XP_024309300.1:p.Asp1536=
XM_024453533.1:c.4578T= XP_024309301.1:p.Asp1526=
XM_024453534.1:c.4401T= XP_024309302.1:p.Asp1467=
XM_024453535.1:c.4371T= XP_024309303.1:p.Asp1457=
XM_024453536.1:c.4578T= XP_024309304.1:p.Asp1526=
XM_024453537.1:c.4578T= XP_024309305.1:p.Asp1526=
NM_001321309.2:c.4050T= NP_001308238.1:p.Asp1350=
NM_053025.4:c.4578T= MANE Select NP_444253.3:p.Asp1526=
NM_053026.4:c.4371T= NP_444254.3:p.Asp1457=
NM_053027.4:c.4578T= NP_444255.3:p.Asp1526=
NM_053028.4:c.4371T= NP_444256.3:p.Asp1457=