Canonical Allele Identifier: CA1528949144
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871526_14871533delinsACGGGGCG , CM000667.2:g.14871526_14871533delinsACGGGGCG GRCh38
NC_000005.9:g.14871635_14871642delinsACGGGGCG , CM000667.1:g.14871635_14871642delinsACGGGGCG GRCh37
NC_000005.8:g.14924635_14924642delinsACGGGGCG NCBI36
NG_008273.1:g.5246_5253delinsCGCCCCGT
NG_008273.2:g.5253_5260delinsCGCCCCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-86_-79delinsCGCCCCGT MANE Select ENSP00000284268.6:n.-86_-79delinsCGCCCCGT
ENST00000284268.6:c.-86_-79delinsCGCCCCGT ENSP00000284268.6:n.-86_-79delinsCGCCCCGT
ENST00000505140.1:c.-86_-79delinsCGCCCCGT ENSP00000426332.1:n.-86_-79delinsCGCCCCGT
NM_054027.4:c.-86_-79delinsCGCCCCGT NP_473368.1:n.-86_-79delinsCGCCCCGT
XM_011514067.1:c.-86_-79delinsCGCCCCGT XP_011512369.1:n.-86_-79delinsCGCCCCGT
NM_054027.5:c.-86_-79delinsCGCCCCGT NP_473368.1:n.-86_-79delinsCGCCCCGT
NM_054027.6:c.-86_-79delinsCGCCCCGT MANE Select NP_473368.1:n.-86_-79delinsCGCCCCGT