Canonical Allele Identifier: CA359286078

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14871506C>G (hg19) ; chr5:g.14871397C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871397C>G , CM000667.2:g.14871397C>G	GRCh38
NC_000005.9:g.14871506C>G , CM000667.1:g.14871506C>G	GRCh37
NC_000005.8:g.14924506C>G	NCBI36
NG_008273.1:g.5382G>C
NG_008273.2:g.5389G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.51G>C MANE Select	ENSP00000284268.6:p.Leu17Phe
ENST00000284268.6:c.51G>C	ENSP00000284268.6:p.Leu17Phe
ENST00000505140.1:c.51G>C	ENSP00000426332.1:p.Leu17Phe
ENST00000513115.1:n.76G>C
NM_054027.4:c.51G>C	NP_473368.1:p.Leu17Phe
XM_011514067.1:c.51G>C	XP_011512369.1:p.Leu17Phe
NM_054027.5:c.51G>C	NP_473368.1:p.Leu17Phe
NM_054027.6:c.51G>C MANE Select	NP_473368.1:p.Leu17Phe