Canonical Allele Identifier: CA1967915052

Gene: ALX4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44265114C= , CM000673.2:g.44265114C=	GRCh38
NC_000011.9:g.44286664C= , CM000673.1:g.44286664C=	GRCh37
NC_000011.8:g.44243240C=	NCBI36
NG_015809.1:g.50053G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000652299.1:c.976G= MANE Select	ENSP00000498217.1:p.Asp326=
ENST00000329255.3:c.976G=	ENSP00000332744.3:p.Asp326=
NM_021926.3:c.976G=	NP_068745.2:p.Asp326=
XM_011520265.1:c.454G=	XP_011518567.1:p.Asp152=
XM_011520266.1:c.454G=	XP_011518568.1:p.Asp152=
NM_021926.4:c.976G= MANE Select	NP_068745.2:p.Asp326=