Canonical Allele Identifier: CA1398518110
Gene: MYLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123707987G= , CM000665.2:g.123707987G= GRCh38
NC_000003.11:g.123426834G= , CM000665.1:g.123426834G= GRCh37
NC_000003.10:g.124909524G= NCBI36
NG_029111.1:g.181316C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000346322.10:c.1950C= ENSP00000320622.6:p.Thr650=
ENST00000686406.1:c.2157C= ENSP00000509044.1:p.Thr719=
ENST00000686761.1:c.2157C= ENSP00000508758.1:p.Thr719=
ENST00000686822.1:n.2051C=
ENST00000687848.1:c.2187C= ENSP00000508761.1:p.Thr729=
ENST00000690457.1:c.1395C= ENSP00000508777.1:p.Thr465=
ENST00000693689.1:c.1950C= ENSP00000510503.1:p.Thr650=
ENST00000360304.8:c.2157C= MANE Select ENSP00000353452.3:p.Thr719=
ENST00000346322.9:c.1950C= ENSP00000320622.5:p.Thr650=
ENST00000354792.9:c.1950C= ENSP00000346846.6:p.Thr650=
ENST00000359169.5:c.2157C= ENSP00000352088.1:p.Thr719=
ENST00000360304.7:c.2157C= ENSP00000353452.3:p.Thr719=
ENST00000360772.7:c.2157C= ENSP00000354004.3:p.Thr719=
ENST00000464489.5:c.*1736C= ENSP00000417798.1:n.*1736C=
ENST00000475616.5:c.2157C= ENSP00000418335.1:p.Thr719=
NM_053025.3:c.2157C= NP_444253.3:p.Thr719=
NM_053026.3:c.1950C= NP_444254.3:p.Thr650=
NM_053027.3:c.2157C= NP_444255.3:p.Thr719=
NM_053028.3:c.1950C= NP_444256.3:p.Thr650=
XM_011512860.1:c.2157C= XP_011511162.1:p.Thr719=
XM_011512861.1:c.2157C= XP_011511163.1:p.Thr719=
XM_011512862.1:c.1629C= XP_011511164.1:p.Thr543=
XR_241556.2:n.313+3978G=
XR_427403.2:n.406+3978G=
XR_924414.1:n.406+3978G=
XR_924415.1:n.403+3978G=
XR_924416.1:n.230+3978G=
XR_924417.1:n.226+3978G=
XR_924418.1:n.406+3978G=
NM_001321309.1:c.1629C= NP_001308238.1:p.Thr543=
XM_011512860.3:c.2187C= XP_011511162.2:p.Thr729=
XM_011512861.3:c.2187C= XP_011511163.2:p.Thr729=
XM_024453532.1:c.2187C= XP_024309300.1:p.Thr729=
XM_024453533.1:c.2157C= XP_024309301.1:p.Thr719=
XM_024453534.1:c.1980C= XP_024309302.1:p.Thr660=
XM_024453535.1:c.1950C= XP_024309303.1:p.Thr650=
XM_024453536.1:c.2157C= XP_024309304.1:p.Thr719=
XM_024453537.1:c.2157C= XP_024309305.1:p.Thr719=
XR_001740871.2:n.406+3978G=
XR_427403.4:n.406+3978G=
XR_924414.3:n.406+3978G=
XR_924417.3:n.251+3978G=
XR_924418.3:n.406+3978G=
NM_001321309.2:c.1629C= NP_001308238.1:p.Thr543=
NM_053025.4:c.2157C= MANE Select NP_444253.3:p.Thr719=
NM_053026.4:c.1950C= NP_444254.3:p.Thr650=
NM_053027.4:c.2157C= NP_444255.3:p.Thr719=
NM_053028.4:c.1950C= NP_444256.3:p.Thr650=