Canonical Allele Identifier: CA1967915002

Gene: ALX4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44265109C= , CM000673.2:g.44265109C=	GRCh38
NC_000011.9:g.44286659C= , CM000673.1:g.44286659C=	GRCh37
NC_000011.8:g.44243235C=	NCBI36
NG_015809.1:g.50058G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000652299.1:c.981G= MANE Select	ENSP00000498217.1:p.Pro327=
ENST00000329255.3:c.981G=	ENSP00000332744.3:p.Pro327=
NM_021926.3:c.981G=	NP_068745.2:p.Pro327=
XM_011520265.1:c.459G=	XP_011518567.1:p.Pro153=
XM_011520266.1:c.459G=	XP_011518568.1:p.Pro153=
NM_021926.4:c.981G= MANE Select	NP_068745.2:p.Pro327=