Canonical Allele Identifier: CA1528880792

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14716775C= , CM000667.2:g.14716775C=	GRCh38
NC_000005.9:g.14716884C= , CM000667.1:g.14716884C=	GRCh37
NC_000005.8:g.14769884C=	NCBI36
NG_008273.1:g.160004G=
NG_008273.2:g.160011G=
NG_051625.1:g.60982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.1072G= MANE Select	ENSP00000284268.6:p.Gly358=
ENST00000284268.6:c.1072G=	ENSP00000284268.6:p.Gly358=
ENST00000502585.1:n.314G=
NM_054027.4:c.1072G=	NP_473368.1:p.Gly358=
NM_054027.5:c.1072G=	NP_473368.1:p.Gly358=
XM_017009644.2:c.988G=	XP_016865133.1:p.Gly330=
NM_054027.6:c.1072G= MANE Select	NP_473368.1:p.Gly358=