Canonical Allele Identifier: CA359286109

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14871522G>T (hg19) ; chr5:g.14871413G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871413G>T , CM000667.2:g.14871413G>T	GRCh38
NC_000005.9:g.14871522G>T , CM000667.1:g.14871522G>T	GRCh37
NC_000005.8:g.14924522G>T	NCBI36
NG_008273.1:g.5366C>A
NG_008273.2:g.5373C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.35C>A MANE Select	ENSP00000284268.6:p.Pro12His
ENST00000284268.6:c.35C>A	ENSP00000284268.6:p.Pro12His
ENST00000505140.1:c.35C>A	ENSP00000426332.1:p.Pro12His
ENST00000513115.1:n.60C>A
NM_054027.4:c.35C>A	NP_473368.1:p.Pro12His
XM_011514067.1:c.35C>A	XP_011512369.1:p.Pro12His
NM_054027.5:c.35C>A	NP_473368.1:p.Pro12His
NM_054027.6:c.35C>A MANE Select	NP_473368.1:p.Pro12His