Canonical Allele Identifier: CA1398493150

Gene: MYLK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123647305A= , CM000665.2:g.123647305A=	GRCh38
NC_000003.11:g.123366152A= , CM000665.1:g.123366152A=	GRCh37
NC_000003.10:g.124848842A=	NCBI36
NG_029111.1:g.241998T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346322.10:c.4331T=	ENSP00000320622.6:p.Met1444=
ENST00000508240.2:c.938T=	ENSP00000422984.2:p.Met313=
ENST00000513111.2:n.668T=
ENST00000684879.1:n.2170T=
ENST00000685021.1:c.1772T=	ENSP00000508447.1:p.Met591=
ENST00000685259.1:c.2057T=
ENST00000685907.1:n.2319T=
ENST00000685953.1:c.938T=	ENSP00000510593.1:p.Met313=
ENST00000686039.1:c.1922T=
ENST00000686245.1:c.1655T=	ENSP00000509313.1:p.Met552=
ENST00000686406.1:c.4538T=	ENSP00000509044.1:p.Met1513=
ENST00000686458.1:n.1040T=
ENST00000686761.1:c.4538T=	ENSP00000508758.1:p.Met1513=
ENST00000686822.1:n.4432T=
ENST00000687434.1:c.*754T=	ENSP00000509751.1:n.*754T=
ENST00000687709.1:n.2593T=
ENST00000687848.1:c.4568T=	ENSP00000508761.1:p.Met1523=
ENST00000688024.1:c.1772T=	ENSP00000509803.1:p.Met591=
ENST00000688223.1:c.1649+1666T=	ENSP00000508935.1:n.1649+1666T=
ENST00000689868.1:n.2266T=
ENST00000689918.1:n.613T=
ENST00000690086.1:n.639T=
ENST00000690167.1:n.2209T=
ENST00000690457.1:c.3776T=	ENSP00000508777.1:p.Met1259=
ENST00000690534.1:n.1059T=
ENST00000691933.1:c.2162T=
ENST00000692352.1:c.2076T=
ENST00000693689.1:c.4331T=	ENSP00000510503.1:p.Met1444=
ENST00000360304.8:c.4538T= MANE Select	ENSP00000353452.3:p.Met1513=
ENST00000346322.9:c.4331T=	ENSP00000320622.5:p.Met1444=
ENST00000354792.9:c.4331T=	ENSP00000346846.6:p.Met1444=
ENST00000359169.5:c.4538T=	ENSP00000352088.1:p.Met1513=
ENST00000360304.7:c.4538T=	ENSP00000353452.3:p.Met1513=
ENST00000360772.7:c.4538T=	ENSP00000354004.3:p.Met1513=
ENST00000464489.5:c.*4117T=	ENSP00000417798.1:n.*4117T=
ENST00000475616.5:c.4538T=	ENSP00000418335.1:p.Met1513=
ENST00000513111.1:n.250T=
ENST00000514895.5:n.94+1666T=
NM_053025.3:c.4538T=	NP_444253.3:p.Met1513=
NM_053026.3:c.4331T=	NP_444254.3:p.Met1444=
NM_053027.3:c.4538T=	NP_444255.3:p.Met1513=
NM_053028.3:c.4331T=	NP_444256.3:p.Met1444=
XM_011512860.1:c.4538T=	XP_011511162.1:p.Met1513=
XM_011512861.1:c.4415+1666T=	XP_011511163.1:n.4415+1666T=
XM_011512862.1:c.4010T=	XP_011511164.1:p.Met1337=
NM_001321309.1:c.4010T=	NP_001308238.1:p.Met1337=
XM_011512860.3:c.4568T=	XP_011511162.2:p.Met1523=
XM_011512861.3:c.4445+1666T=	XP_011511163.2:n.4445+1666T=
XM_017006469.2:c.1772T=	XP_016861958.1:p.Met591=
XM_017006470.2:c.938T=	XP_016861959.1:p.Met313=
XM_017006471.2:c.938T=	XP_016861960.1:p.Met313=
XM_024453532.1:c.4568T=	XP_024309300.1:p.Met1523=
XM_024453533.1:c.4538T=	XP_024309301.1:p.Met1513=
XM_024453534.1:c.4361T=	XP_024309302.1:p.Met1454=
XM_024453535.1:c.4331T=	XP_024309303.1:p.Met1444=
XM_024453536.1:c.4538T=	XP_024309304.1:p.Met1513=
XM_024453537.1:c.4538T=	XP_024309305.1:p.Met1513=
NM_001321309.2:c.4010T=	NP_001308238.1:p.Met1337=
NM_053025.4:c.4538T= MANE Select	NP_444253.3:p.Met1513=
NM_053026.4:c.4331T=	NP_444254.3:p.Met1444=
NM_053027.4:c.4538T=	NP_444255.3:p.Met1513=
NM_053028.4:c.4331T=	NP_444256.3:p.Met1444=