Canonical Allele Identifier: CA1528949176
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871537G= , CM000667.2:g.14871537G= GRCh38
NC_000005.9:g.14871646G= , CM000667.1:g.14871646G= GRCh37
NC_000005.8:g.14924646G= NCBI36
NG_008273.1:g.5242C=
NG_008273.2:g.5249C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-90C= MANE Select ENSP00000284268.6:n.-90C=
ENST00000284268.6:c.-90C= ENSP00000284268.6:n.-90C=
ENST00000505140.1:c.-90C= ENSP00000426332.1:n.-90C=
NM_054027.4:c.-90C= NP_473368.1:n.-90C=
XM_011514067.1:c.-90C= XP_011512369.1:n.-90C=
NM_054027.5:c.-90C= NP_473368.1:n.-90C=
NM_054027.6:c.-90C= MANE Select NP_473368.1:n.-90C=