Canonical Allele Identifier: CA359285996

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14871468C>A (hg19) ; chr5:g.14871359C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871359C>A , CM000667.2:g.14871359C>A	GRCh38
NC_000005.9:g.14871468C>A , CM000667.1:g.14871468C>A	GRCh37
NC_000005.8:g.14924468C>A	NCBI36
NG_008273.1:g.5420G>T
NG_008273.2:g.5427G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.89G>T MANE Select	ENSP00000284268.6:p.Gly30Val
ENST00000284268.6:c.89G>T	ENSP00000284268.6:p.Gly30Val
ENST00000505140.1:c.89G>T	ENSP00000426332.1:p.Gly30Val
ENST00000513115.1:n.114G>T
NM_054027.4:c.89G>T	NP_473368.1:p.Gly30Val
XM_011514067.1:c.89G>T	XP_011512369.1:p.Gly30Val
NM_054027.5:c.89G>T	NP_473368.1:p.Gly30Val
NM_054027.6:c.89G>T MANE Select	NP_473368.1:p.Gly30Val