Canonical Allele Identifier: CA1528949011

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871315A= , CM000667.2:g.14871315A=	GRCh38
NC_000005.9:g.14871424A= , CM000667.1:g.14871424A=	GRCh37
NC_000005.8:g.14924424A=	NCBI36
NG_008273.1:g.5464T=
NG_008273.2:g.5471T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.96+37T= MANE Select	ENSP00000284268.6:n.96+37T=
ENST00000284268.6:c.96+37T=	ENSP00000284268.6:n.96+37T=
ENST00000505140.1:c.133T=	ENSP00000426332.1:p.Cys45=
ENST00000513115.1:n.121+37T=
NM_054027.4:c.96+37T=	NP_473368.1:n.96+37T=
XM_011514067.1:c.96+37T=	XP_011512369.1:n.96+37T=
NM_054027.5:c.96+37T=	NP_473368.1:n.96+37T=
NM_054027.6:c.96+37T= MANE Select	NP_473368.1:n.96+37T=