Canonical Allele Identifier: CA1528949146
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871526_14871527delinsAC , CM000667.2:g.14871526_14871527delinsAC GRCh38
NC_000005.9:g.14871635_14871636delinsAC , CM000667.1:g.14871635_14871636delinsAC GRCh37
NC_000005.8:g.14924635_14924636delinsAC NCBI36
NG_008273.1:g.5252_5253delinsGT
NG_008273.2:g.5259_5260delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-80_-79delinsGT MANE Select ENSP00000284268.6:n.-80_-79delinsGT
ENST00000284268.6:c.-80_-79delinsGT ENSP00000284268.6:n.-80_-79delinsGT
ENST00000505140.1:c.-80_-79delinsGT ENSP00000426332.1:n.-80_-79delinsGT
NM_054027.4:c.-80_-79delinsGT NP_473368.1:n.-80_-79delinsGT
XM_011514067.1:c.-80_-79delinsGT XP_011512369.1:n.-80_-79delinsGT
NM_054027.5:c.-80_-79delinsGT NP_473368.1:n.-80_-79delinsGT
NM_054027.6:c.-80_-79delinsGT MANE Select NP_473368.1:n.-80_-79delinsGT