Canonical Allele Identifier: CA443295600

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14716882T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14716773T>G , CM000667.2:g.14716773T>G	GRCh38
NC_000005.9:g.14716882T>G , CM000667.1:g.14716882T>G	GRCh37
NC_000005.8:g.14769882T>G	NCBI36
NG_008273.1:g.160006A>C
NG_008273.2:g.160013A>C
NG_051625.1:g.60980T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.1074A>C MANE Select	ENSP00000284268.6:p.Gly358=
ENST00000284268.6:c.1074A>C	ENSP00000284268.6:p.Gly358=
ENST00000502585.1:n.316A>C
NM_054027.4:c.1074A>C	NP_473368.1:p.Gly358=
NM_054027.5:c.1074A>C	NP_473368.1:p.Gly358=
XM_017009644.2:c.990A>C	XP_016865133.1:p.Gly330=
NM_054027.6:c.1074A>C MANE Select	NP_473368.1:p.Gly358=