Canonical Allele Identifier: CA1398493129

Gene: MYLK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123647241G= , CM000665.2:g.123647241G=	GRCh38
NC_000003.11:g.123366088G= , CM000665.1:g.123366088G=	GRCh37
NC_000003.10:g.124848778G=	NCBI36
NG_029111.1:g.242062C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.4395C=	ENSP00000320622.6:p.Ile1465=
ENST00000508240.2:c.1002C=	ENSP00000422984.2:p.Ile334=
ENST00000513111.2:n.732C=
ENST00000684879.1:n.2234C=
ENST00000685021.1:c.1836C=	ENSP00000508447.1:p.Ile612=
ENST00000685259.1:c.2121C=
ENST00000685907.1:n.2383C=
ENST00000685953.1:c.1002C=	ENSP00000510593.1:p.Ile334=
ENST00000686039.1:c.1986C=
ENST00000686245.1:c.1719C=	ENSP00000509313.1:p.Ile573=
ENST00000686406.1:c.4602C=	ENSP00000509044.1:p.Ile1534=
ENST00000686458.1:n.1104C=
ENST00000686761.1:c.4602C=	ENSP00000508758.1:p.Ile1534=
ENST00000686822.1:n.4496C=
ENST00000687434.1:c.*818C=	ENSP00000509751.1:n.*818C=
ENST00000687709.1:n.2657C=
ENST00000687848.1:c.4632C=	ENSP00000508761.1:p.Ile1544=
ENST00000688024.1:c.1836C=	ENSP00000509803.1:p.Ile612=
ENST00000688223.1:c.1649+1730C=	ENSP00000508935.1:n.1649+1730C=
ENST00000689868.1:n.2330C=
ENST00000689918.1:n.677C=
ENST00000690086.1:n.703C=
ENST00000690167.1:n.2273C=
ENST00000690457.1:c.3840C=	ENSP00000508777.1:p.Ile1280=
ENST00000690534.1:n.1123C=
ENST00000691933.1:c.2226C=
ENST00000692352.1:c.2140C=
ENST00000693689.1:c.4395C=	ENSP00000510503.1:p.Ile1465=
ENST00000360304.8:c.4602C= MANE Select	ENSP00000353452.3:p.Ile1534=
ENST00000346322.9:c.4395C=	ENSP00000320622.5:p.Ile1465=
ENST00000354792.9:c.4395C=	ENSP00000346846.6:p.Ile1465=
ENST00000359169.5:c.4602C=	ENSP00000352088.1:p.Ile1534=
ENST00000360304.7:c.4602C=	ENSP00000353452.3:p.Ile1534=
ENST00000360772.7:c.4602C=	ENSP00000354004.3:p.Ile1534=
ENST00000464489.5:c.*4181C=	ENSP00000417798.1:n.*4181C=
ENST00000475616.5:c.4602C=	ENSP00000418335.1:p.Ile1534=
ENST00000513111.1:n.314C=
ENST00000514895.5:n.94+1730C=
NM_053025.3:c.4602C=	NP_444253.3:p.Ile1534=
NM_053026.3:c.4395C=	NP_444254.3:p.Ile1465=
NM_053027.3:c.4602C=	NP_444255.3:p.Ile1534=
NM_053028.3:c.4395C=	NP_444256.3:p.Ile1465=
XM_011512860.1:c.4602C=	XP_011511162.1:p.Ile1534=
XM_011512861.1:c.4415+1730C=	XP_011511163.1:n.4415+1730C=
XM_011512862.1:c.4074C=	XP_011511164.1:p.Ile1358=
NM_001321309.1:c.4074C=	NP_001308238.1:p.Ile1358=
XM_011512860.3:c.4632C=	XP_011511162.2:p.Ile1544=
XM_011512861.3:c.4445+1730C=	XP_011511163.2:n.4445+1730C=
XM_017006469.2:c.1836C=	XP_016861958.1:p.Ile612=
XM_017006470.2:c.1002C=	XP_016861959.1:p.Ile334=
XM_017006471.2:c.1002C=	XP_016861960.1:p.Ile334=
XM_024453532.1:c.4632C=	XP_024309300.1:p.Ile1544=
XM_024453533.1:c.4602C=	XP_024309301.1:p.Ile1534=
XM_024453534.1:c.4425C=	XP_024309302.1:p.Ile1475=
XM_024453535.1:c.4395C=	XP_024309303.1:p.Ile1465=
XM_024453536.1:c.4602C=	XP_024309304.1:p.Ile1534=
XM_024453537.1:c.4602C=	XP_024309305.1:p.Ile1534=
NM_001321309.2:c.4074C=	NP_001308238.1:p.Ile1358=
NM_053025.4:c.4602C= MANE Select	NP_444253.3:p.Ile1534=
NM_053026.4:c.4395C=	NP_444254.3:p.Ile1465=
NM_053027.4:c.4602C=	NP_444255.3:p.Ile1534=
NM_053028.4:c.4395C=	NP_444256.3:p.Ile1465=