Canonical Allele Identifier: CA1528949047
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871370G= , CM000667.2:g.14871370G= GRCh38
NC_000005.9:g.14871479G= , CM000667.1:g.14871479G= GRCh37
NC_000005.8:g.14924479G= NCBI36
NG_008273.1:g.5409C=
NG_008273.2:g.5416C=

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.78C= MANE Select ENSP00000284268.6:p.Ala26=
ENST00000284268.6:c.78C= ENSP00000284268.6:p.Ala26=
ENST00000505140.1:c.78C= ENSP00000426332.1:p.Ala26=
ENST00000513115.1:n.103C=
NM_054027.4:c.78C= NP_473368.1:p.Ala26=
XM_011514067.1:c.78C= XP_011512369.1:p.Ala26=
NM_054027.5:c.78C= NP_473368.1:p.Ala26=
NM_054027.6:c.78C= MANE Select NP_473368.1:p.Ala26=