Canonical Allele Identifier: CA2262577616

Gene: MYL4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47221771T= , CM000679.2:g.47221771T=	GRCh38
NC_000017.10:g.45299137T= , CM000679.1:g.45299137T=	GRCh37
NC_000017.9:g.42654136T=	NCBI36
NG_052847.1:g.17755T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354968.5:c.403T=	ENSP00000347055.1:p.Phe135=
ENST00000393450.5:c.403T= MANE Select	ENSP00000377096.1:p.Phe135=
ENST00000536623.6:c.403T=	ENSP00000442375.2:p.Phe135=
ENST00000570671.1:c.114T=
ENST00000570772.5:c.*189T=	ENSP00000458194.1:n.*189T=
ENST00000571981.5:c.*189T=	ENSP00000459035.1:n.*189T=
ENST00000572303.1:c.496T=	ENSP00000461747.1:p.Phe166=
ENST00000572316.5:c.403T=	ENSP00000461570.1:p.Phe135=
ENST00000573747.6:c.*5T=	ENSP00000460734.1:n.*5T=
ENST00000576874.5:c.403T=	ENSP00000458907.1:p.Phe135=
NM_001002841.1:c.403T=	NP_001002841.1:p.Phe135=
NM_002476.2:c.403T= MANE Select	NP_002467.1:p.Phe135=
XM_005257391.3:c.403T=	XP_005257448.1:p.Phe135=
XM_011524838.1:c.403T=	XP_011523140.1:p.Phe135=
XM_011524839.1:c.193T=	XP_011523141.1:p.Phe65=
XM_005257391.5:c.403T=	XP_005257448.1:p.Phe135=
XM_011524839.2:c.496T=	XP_011523141.2:p.Phe166=
XM_017024683.1:c.496T=	XP_016880172.1:p.Phe166=
XM_024450766.1:c.496T=	XP_024306534.1:p.Phe166=
NM_001002841.2:c.403T=	NP_001002841.1:p.Phe135=