Canonical Allele Identifier: CA1967915047

Gene: ALX4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44265110G= , CM000673.2:g.44265110G=	GRCh38
NC_000011.9:g.44286660G= , CM000673.1:g.44286660G=	GRCh37
NC_000011.8:g.44243236G=	NCBI36
NG_015809.1:g.50057C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000652299.1:c.980C= MANE Select	ENSP00000498217.1:p.Pro327=
ENST00000329255.3:c.980C=	ENSP00000332744.3:p.Pro327=
NM_021926.3:c.980C=	NP_068745.2:p.Pro327=
XM_011520265.1:c.458C=	XP_011518567.1:p.Pro153=
XM_011520266.1:c.458C=	XP_011518568.1:p.Pro153=
NM_021926.4:c.980C= MANE Select	NP_068745.2:p.Pro327=