Canonical Allele Identifier: CA1967928956

Gene: ALX4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44275399A= , CM000673.2:g.44275399A=	GRCh38
NC_000011.9:g.44296949A= , CM000673.1:g.44296949A=	GRCh37
NC_000011.8:g.44253525A=	NCBI36
NG_015809.1:g.39768T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000652299.1:c.726T= MANE Select	ENSP00000498217.1:p.Tyr242=
ENST00000329255.3:c.726T=	ENSP00000332744.3:p.Tyr242=
NM_021926.3:c.726T=	NP_068745.2:p.Tyr242=
XM_011520264.1:c.726T=	XP_011518566.1:p.Tyr242=
XM_011520265.1:c.204T=	XP_011518567.1:p.Tyr68=
XM_011520266.1:c.204T=	XP_011518568.1:p.Tyr68=
NM_021926.4:c.726T= MANE Select	NP_068745.2:p.Tyr242=