Canonical Allele Identifier: CA1398493143
Gene: MYLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123647288G= , CM000665.2:g.123647288G= GRCh38
NC_000003.11:g.123366135G= , CM000665.1:g.123366135G= GRCh37
NC_000003.10:g.124848825G= NCBI36
NG_029111.1:g.242015C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000346322.10:c.4348C= ENSP00000320622.6:p.Pro1450=
ENST00000508240.2:c.955C= ENSP00000422984.2:p.Pro319=
ENST00000513111.2:n.685C=
ENST00000684879.1:n.2187C=
ENST00000685021.1:c.1789C= ENSP00000508447.1:p.Pro597=
ENST00000685259.1:c.2074C=
ENST00000685907.1:n.2336C=
ENST00000685953.1:c.955C= ENSP00000510593.1:p.Pro319=
ENST00000686039.1:c.1939C=
ENST00000686245.1:c.1672C= ENSP00000509313.1:p.Pro558=
ENST00000686406.1:c.4555C= ENSP00000509044.1:p.Pro1519=
ENST00000686458.1:n.1057C=
ENST00000686761.1:c.4555C= ENSP00000508758.1:p.Pro1519=
ENST00000686822.1:n.4449C=
ENST00000687434.1:c.*771C= ENSP00000509751.1:n.*771C=
ENST00000687709.1:n.2610C=
ENST00000687848.1:c.4585C= ENSP00000508761.1:p.Pro1529=
ENST00000688024.1:c.1789C= ENSP00000509803.1:p.Pro597=
ENST00000688223.1:c.1649+1683C= ENSP00000508935.1:n.1649+1683C=
ENST00000689868.1:n.2283C=
ENST00000689918.1:n.630C=
ENST00000690086.1:n.656C=
ENST00000690167.1:n.2226C=
ENST00000690457.1:c.3793C= ENSP00000508777.1:p.Pro1265=
ENST00000690534.1:n.1076C=
ENST00000691933.1:c.2179C=
ENST00000692352.1:c.2093C=
ENST00000693689.1:c.4348C= ENSP00000510503.1:p.Pro1450=
ENST00000360304.8:c.4555C= MANE Select ENSP00000353452.3:p.Pro1519=
ENST00000346322.9:c.4348C= ENSP00000320622.5:p.Pro1450=
ENST00000354792.9:c.4348C= ENSP00000346846.6:p.Pro1450=
ENST00000359169.5:c.4555C= ENSP00000352088.1:p.Pro1519=
ENST00000360304.7:c.4555C= ENSP00000353452.3:p.Pro1519=
ENST00000360772.7:c.4555C= ENSP00000354004.3:p.Pro1519=
ENST00000464489.5:c.*4134C= ENSP00000417798.1:n.*4134C=
ENST00000475616.5:c.4555C= ENSP00000418335.1:p.Pro1519=
ENST00000513111.1:n.267C=
ENST00000514895.5:n.94+1683C=
NM_053025.3:c.4555C= NP_444253.3:p.Pro1519=
NM_053026.3:c.4348C= NP_444254.3:p.Pro1450=
NM_053027.3:c.4555C= NP_444255.3:p.Pro1519=
NM_053028.3:c.4348C= NP_444256.3:p.Pro1450=
XM_011512860.1:c.4555C= XP_011511162.1:p.Pro1519=
XM_011512861.1:c.4415+1683C= XP_011511163.1:n.4415+1683C=
XM_011512862.1:c.4027C= XP_011511164.1:p.Pro1343=
NM_001321309.1:c.4027C= NP_001308238.1:p.Pro1343=
XM_011512860.3:c.4585C= XP_011511162.2:p.Pro1529=
XM_011512861.3:c.4445+1683C= XP_011511163.2:n.4445+1683C=
XM_017006469.2:c.1789C= XP_016861958.1:p.Pro597=
XM_017006470.2:c.955C= XP_016861959.1:p.Pro319=
XM_017006471.2:c.955C= XP_016861960.1:p.Pro319=
XM_024453532.1:c.4585C= XP_024309300.1:p.Pro1529=
XM_024453533.1:c.4555C= XP_024309301.1:p.Pro1519=
XM_024453534.1:c.4378C= XP_024309302.1:p.Pro1460=
XM_024453535.1:c.4348C= XP_024309303.1:p.Pro1450=
XM_024453536.1:c.4555C= XP_024309304.1:p.Pro1519=
XM_024453537.1:c.4555C= XP_024309305.1:p.Pro1519=
NM_001321309.2:c.4027C= NP_001308238.1:p.Pro1343=
NM_053025.4:c.4555C= MANE Select NP_444253.3:p.Pro1519=
NM_053026.4:c.4348C= NP_444254.3:p.Pro1450=
NM_053027.4:c.4555C= NP_444255.3:p.Pro1519=
NM_053028.4:c.4348C= NP_444256.3:p.Pro1450=