Canonical Allele Identifier: CA1528949049
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871377T= , CM000667.2:g.14871377T= GRCh38
NC_000005.9:g.14871486T= , CM000667.1:g.14871486T= GRCh37
NC_000005.8:g.14924486T= NCBI36
NG_008273.1:g.5402A=
NG_008273.2:g.5409A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.71A= MANE Select ENSP00000284268.6:p.Asn24=
ENST00000284268.6:c.71A= ENSP00000284268.6:p.Asn24=
ENST00000505140.1:c.71A= ENSP00000426332.1:p.Asn24=
ENST00000513115.1:n.96A=
NM_054027.4:c.71A= NP_473368.1:p.Asn24=
XM_011514067.1:c.71A= XP_011512369.1:p.Asn24=
NM_054027.5:c.71A= NP_473368.1:p.Asn24=
NM_054027.6:c.71A= MANE Select NP_473368.1:p.Asn24=