Canonical Allele Identifier: CA1528949042
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871355C= , CM000667.2:g.14871355C= GRCh38
NC_000005.9:g.14871464C= , CM000667.1:g.14871464C= GRCh37
NC_000005.8:g.14924464C= NCBI36
NG_008273.1:g.5424G=
NG_008273.2:g.5431G=

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.93G= MANE Select ENSP00000284268.6:p.Glu31=
ENST00000284268.6:c.93G= ENSP00000284268.6:p.Glu31=
ENST00000505140.1:c.93G= ENSP00000426332.1:p.Glu31=
ENST00000513115.1:n.118G=
NM_054027.4:c.93G= NP_473368.1:p.Glu31=
XM_011514067.1:c.93G= XP_011512369.1:p.Glu31=
NM_054027.5:c.93G= NP_473368.1:p.Glu31=
NM_054027.6:c.93G= MANE Select NP_473368.1:p.Glu31=