Canonical Allele Identifier: CA1398511299

Gene: MYLK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123692663T= , CM000665.2:g.123692663T=	GRCh38
NC_000003.11:g.123411510T= , CM000665.1:g.123411510T=	GRCh37
NC_000003.10:g.124894200T=	NCBI36
NG_029111.1:g.196640A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.3358+72A=	ENSP00000320622.6:n.3358+72A=
ENST00000504946.6:c.1175+72A=
ENST00000684879.1:n.1197+72A=
ENST00000685021.1:c.799+72A=	ENSP00000508447.1:n.799+72A=
ENST00000685259.1:c.1103+72A=
ENST00000685907.1:n.1346+72A=
ENST00000686039.1:c.1103+72A=
ENST00000686245.1:c.682+7357A=	ENSP00000509313.1:n.682+7357A=
ENST00000686406.1:c.3565+72A=	ENSP00000509044.1:n.3565+72A=
ENST00000686761.1:c.3565+72A=	ENSP00000508758.1:n.3565+72A=
ENST00000686822.1:n.3459+72A=
ENST00000687709.1:n.830+72A=
ENST00000687848.1:c.3595+72A=	ENSP00000508761.1:n.3595+72A=
ENST00000688024.1:c.799+72A=	ENSP00000509803.1:n.799+72A=
ENST00000688223.1:c.799+72A=	ENSP00000508935.1:n.799+72A=
ENST00000689227.1:c.1238+72A=
ENST00000689868.1:n.1293+72A=
ENST00000690167.1:n.1236+72A=
ENST00000690457.1:c.2803+72A=	ENSP00000508777.1:n.2803+72A=
ENST00000691933.1:c.1103+72A=
ENST00000692352.1:c.1103+72A=
ENST00000693689.1:c.3358+72A=	ENSP00000510503.1:n.3358+72A=
ENST00000360304.8:c.3565+72A= MANE Select	ENSP00000353452.3:n.3565+72A=
ENST00000346322.9:c.3358+72A=	ENSP00000320622.5:n.3358+72A=
ENST00000354792.9:c.3358+72A=	ENSP00000346846.6:n.3358+72A=
ENST00000359169.5:c.3565+72A=	ENSP00000352088.1:n.3565+72A=
ENST00000360304.7:c.3565+72A=	ENSP00000353452.3:n.3565+72A=
ENST00000360772.7:c.3565+72A=	ENSP00000354004.3:n.3565+72A=
ENST00000464489.5:c.*3144+72A=	ENSP00000417798.1:n.*3144+72A=
ENST00000475616.5:c.3565+72A=	ENSP00000418335.1:n.3565+72A=
ENST00000504946.5:n.1123+72A=
ENST00000510775.5:n.283+72A=
NM_053025.3:c.3565+72A=	NP_444253.3:n.3565+72A=
NM_053026.3:c.3358+72A=	NP_444254.3:n.3358+72A=
NM_053027.3:c.3565+72A=	NP_444255.3:n.3565+72A=
NM_053028.3:c.3358+72A=	NP_444256.3:n.3358+72A=
XM_011512860.1:c.3565+72A=	XP_011511162.1:n.3565+72A=
XM_011512861.1:c.3565+72A=	XP_011511163.1:n.3565+72A=
XM_011512862.1:c.3037+72A=	XP_011511164.1:n.3037+72A=
NM_001321309.1:c.3037+72A=	NP_001308238.1:n.3037+72A=
XM_011512860.3:c.3595+72A=	XP_011511162.2:n.3595+72A=
XM_011512861.3:c.3595+72A=	XP_011511163.2:n.3595+72A=
XM_017006469.2:c.799+72A=	XP_016861958.1:n.799+72A=
XM_024453532.1:c.3595+72A=	XP_024309300.1:n.3595+72A=
XM_024453533.1:c.3565+72A=	XP_024309301.1:n.3565+72A=
XM_024453534.1:c.3388+72A=	XP_024309302.1:n.3388+72A=
XM_024453535.1:c.3358+72A=	XP_024309303.1:n.3358+72A=
XM_024453536.1:c.3565+72A=	XP_024309304.1:n.3565+72A=
XM_024453537.1:c.3565+72A=	XP_024309305.1:n.3565+72A=
NM_001321309.2:c.3037+72A=	NP_001308238.1:n.3037+72A=
NM_053025.4:c.3565+72A= MANE Select	NP_444253.3:n.3565+72A=
NM_053026.4:c.3358+72A=	NP_444254.3:n.3358+72A=
NM_053027.4:c.3565+72A=	NP_444255.3:n.3565+72A=
NM_053028.4:c.3358+72A=	NP_444256.3:n.3358+72A=