Canonical Allele Identifier: CA443372216

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14871497C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871388C>G , CM000667.2:g.14871388C>G	GRCh38
NC_000005.9:g.14871497C>G , CM000667.1:g.14871497C>G	GRCh37
NC_000005.8:g.14924497C>G	NCBI36
NG_008273.1:g.5391G>C
NG_008273.2:g.5398G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.60G>C MANE Select	ENSP00000284268.6:p.Leu20=
ENST00000284268.6:c.60G>C	ENSP00000284268.6:p.Leu20=
ENST00000505140.1:c.60G>C	ENSP00000426332.1:p.Leu20=
ENST00000513115.1:n.85G>C
NM_054027.4:c.60G>C	NP_473368.1:p.Leu20=
XM_011514067.1:c.60G>C	XP_011512369.1:p.Leu20=
NM_054027.5:c.60G>C	NP_473368.1:p.Leu20=
NM_054027.6:c.60G>C MANE Select	NP_473368.1:p.Leu20=