Canonical Allele Identifier: CA1398511335
Gene: MYLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123692745G= , CM000665.2:g.123692745G= GRCh38
NC_000003.11:g.123411592G= , CM000665.1:g.123411592G= GRCh37
NC_000003.10:g.124894282G= NCBI36
NG_029111.1:g.196558C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000346322.10:c.3348C= ENSP00000320622.6:p.Val1116=
ENST00000504946.6:c.1165C=
ENST00000684879.1:n.1187C=
ENST00000685021.1:c.789C= ENSP00000508447.1:p.Val263=
ENST00000685259.1:c.1093C=
ENST00000685907.1:n.1336C=
ENST00000686039.1:c.1093C=
ENST00000686245.1:c.682+7275C= ENSP00000509313.1:n.682+7275C=
ENST00000686406.1:c.3555C= ENSP00000509044.1:p.Val1185=
ENST00000686761.1:c.3555C= ENSP00000508758.1:p.Val1185=
ENST00000686822.1:n.3449C=
ENST00000687709.1:n.820C=
ENST00000687848.1:c.3585C= ENSP00000508761.1:p.Val1195=
ENST00000688024.1:c.789C= ENSP00000509803.1:p.Val263=
ENST00000688223.1:c.789C= ENSP00000508935.1:p.Val263=
ENST00000689227.1:c.1228C=
ENST00000689868.1:n.1283C=
ENST00000690167.1:n.1226C=
ENST00000690457.1:c.2793C= ENSP00000508777.1:p.Val931=
ENST00000691933.1:c.1093C=
ENST00000692352.1:c.1093C=
ENST00000693689.1:c.3348C= ENSP00000510503.1:p.Val1116=
ENST00000360304.8:c.3555C= MANE Select ENSP00000353452.3:p.Val1185=
ENST00000346322.9:c.3348C= ENSP00000320622.5:p.Val1116=
ENST00000354792.9:c.3348C= ENSP00000346846.6:p.Val1116=
ENST00000359169.5:c.3555C= ENSP00000352088.1:p.Val1185=
ENST00000360304.7:c.3555C= ENSP00000353452.3:p.Val1185=
ENST00000360772.7:c.3555C= ENSP00000354004.3:p.Val1185=
ENST00000464489.5:c.*3134C= ENSP00000417798.1:n.*3134C=
ENST00000475616.5:c.3555C= ENSP00000418335.1:p.Val1185=
ENST00000503644.1:n.224C=
ENST00000504946.5:n.1113C=
ENST00000510775.5:n.273C=
NM_053025.3:c.3555C= NP_444253.3:p.Val1185=
NM_053026.3:c.3348C= NP_444254.3:p.Val1116=
NM_053027.3:c.3555C= NP_444255.3:p.Val1185=
NM_053028.3:c.3348C= NP_444256.3:p.Val1116=
XM_011512860.1:c.3555C= XP_011511162.1:p.Val1185=
XM_011512861.1:c.3555C= XP_011511163.1:p.Val1185=
XM_011512862.1:c.3027C= XP_011511164.1:p.Val1009=
NM_001321309.1:c.3027C= NP_001308238.1:p.Val1009=
XM_011512860.3:c.3585C= XP_011511162.2:p.Val1195=
XM_011512861.3:c.3585C= XP_011511163.2:p.Val1195=
XM_017006469.2:c.789C= XP_016861958.1:p.Val263=
XM_024453532.1:c.3585C= XP_024309300.1:p.Val1195=
XM_024453533.1:c.3555C= XP_024309301.1:p.Val1185=
XM_024453534.1:c.3378C= XP_024309302.1:p.Val1126=
XM_024453535.1:c.3348C= XP_024309303.1:p.Val1116=
XM_024453536.1:c.3555C= XP_024309304.1:p.Val1185=
XM_024453537.1:c.3555C= XP_024309305.1:p.Val1185=
NM_001321309.2:c.3027C= NP_001308238.1:p.Val1009=
NM_053025.4:c.3555C= MANE Select NP_444253.3:p.Val1185=
NM_053026.4:c.3348C= NP_444254.3:p.Val1116=
NM_053027.4:c.3555C= NP_444255.3:p.Val1185=
NM_053028.4:c.3348C= NP_444256.3:p.Val1116=