Canonical Allele Identifier: CA1528880901

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14716976A= , CM000667.2:g.14716976A=	GRCh38
NC_000005.9:g.14717085A= , CM000667.1:g.14717085A=	GRCh37
NC_000005.8:g.14770085A=	NCBI36
NG_008273.1:g.159803T=
NG_008273.2:g.159810T=
NG_051625.1:g.61183A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.1012-141T= MANE Select	ENSP00000284268.6:n.1012-141T=
ENST00000284268.6:c.1012-141T=	ENSP00000284268.6:n.1012-141T=
ENST00000502585.1:n.113T=
NM_054027.4:c.1012-141T=	NP_473368.1:n.1012-141T=
NM_054027.5:c.1012-141T=	NP_473368.1:n.1012-141T=
XM_017009644.2:c.928-141T=	XP_016865133.1:n.928-141T=
NM_054027.6:c.1012-141T= MANE Select	NP_473368.1:n.1012-141T=