Canonical Allele Identifier: CA1528949149

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871526_14871528delinsACG , CM000667.2:g.14871526_14871528delinsACG	GRCh38
NC_000005.9:g.14871635_14871637delinsACG , CM000667.1:g.14871635_14871637delinsACG	GRCh37
NC_000005.8:g.14924635_14924637delinsACG	NCBI36
NG_008273.1:g.5251_5253delinsCGT
NG_008273.2:g.5258_5260delinsCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.-81_-79delinsCGT MANE Select	ENSP00000284268.6:n.-81_-79delinsCGT
ENST00000284268.6:c.-81_-79delinsCGT	ENSP00000284268.6:n.-81_-79delinsCGT
ENST00000505140.1:c.-81_-79delinsCGT	ENSP00000426332.1:n.-81_-79delinsCGT
NM_054027.4:c.-81_-79delinsCGT	NP_473368.1:n.-81_-79delinsCGT
XM_011514067.1:c.-81_-79delinsCGT	XP_011512369.1:n.-81_-79delinsCGT
NM_054027.5:c.-81_-79delinsCGT	NP_473368.1:n.-81_-79delinsCGT
NM_054027.6:c.-81_-79delinsCGT MANE Select	NP_473368.1:n.-81_-79delinsCGT