Canonical Allele Identifier: CA1528949110

Gene: ANKH

Linked Data

• dbSNP Id: rs1735824100

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871490A>G , CM000667.2:g.14871490A>G	GRCh38
NC_000005.9:g.14871599A>G , CM000667.1:g.14871599A>G	GRCh37
NC_000005.8:g.14924599A>G	NCBI36
NG_008273.1:g.5289T>C
NG_008273.2:g.5296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.-43T>C MANE Select	ENSP00000284268.6:n.-43T>C
ENST00000284268.6:c.-43T>C	ENSP00000284268.6:n.-43T>C
ENST00000505140.1:c.-43T>C	ENSP00000426332.1:n.-43T>C
NM_054027.4:c.-43T>C	NP_473368.1:n.-43T>C
XM_011514067.1:c.-43T>C	XP_011512369.1:n.-43T>C
NM_054027.5:c.-43T>C	NP_473368.1:n.-43T>C
NM_054027.6:c.-43T>C MANE Select	NP_473368.1:n.-43T>C