Canonical Allele Identifier: CA2765375262
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871551_14871552insGC , CM000667.2:g.14871551_14871552insGC GRCh38
NC_000005.9:g.14871660_14871661insGC , CM000667.1:g.14871660_14871661insGC GRCh37
NC_000005.8:g.14924660_14924661insGC NCBI36
NG_008273.1:g.5228_5229insCG
NG_008273.2:g.5235_5236insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-104_-103insCG MANE Select ENSP00000284268.6:n.-104_-103insCG
ENST00000284268.6:c.-104_-103insCG ENSP00000284268.6:n.-104_-103insCG
ENST00000505140.1:c.-104_-103insCG ENSP00000426332.1:n.-104_-103insCG
NM_054027.4:c.-104_-103insCG NP_473368.1:n.-104_-103insCG
XM_011514067.1:c.-104_-103insCG XP_011512369.1:n.-104_-103insCG
NM_054027.5:c.-104_-103insCG NP_473368.1:n.-104_-103insCG
NM_054027.6:c.-104_-103insCG MANE Select NP_473368.1:n.-104_-103insCG