Canonical Allele Identifier: CA1967915056

Gene: ALX4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44265115G= , CM000673.2:g.44265115G=	GRCh38
NC_000011.9:g.44286665G= , CM000673.1:g.44286665G=	GRCh37
NC_000011.8:g.44243241G=	NCBI36
NG_015809.1:g.50052C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000652299.1:c.975C= MANE Select	ENSP00000498217.1:p.Cys325=
ENST00000329255.3:c.975C=	ENSP00000332744.3:p.Cys325=
NM_021926.3:c.975C=	NP_068745.2:p.Cys325=
XM_011520265.1:c.453C=	XP_011518567.1:p.Cys151=
XM_011520266.1:c.453C=	XP_011518568.1:p.Cys151=
NM_021926.4:c.975C= MANE Select	NP_068745.2:p.Cys325=