Canonical Allele Identifier: CA1528949032

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871337G= , CM000667.2:g.14871337G=	GRCh38
NC_000005.9:g.14871446G= , CM000667.1:g.14871446G=	GRCh37
NC_000005.8:g.14924446G=	NCBI36
NG_008273.1:g.5442C=
NG_008273.2:g.5449C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.96+15C= MANE Select	ENSP00000284268.6:n.96+15C=
ENST00000284268.6:c.96+15C=	ENSP00000284268.6:n.96+15C=
ENST00000505140.1:c.111C=	ENSP00000426332.1:p.Pro37=
ENST00000513115.1:n.121+15C=
NM_054027.4:c.96+15C=	NP_473368.1:n.96+15C=
XM_011514067.1:c.96+15C=	XP_011512369.1:n.96+15C=
NM_054027.5:c.96+15C=	NP_473368.1:n.96+15C=
NM_054027.6:c.96+15C= MANE Select	NP_473368.1:n.96+15C=