Canonical Allele Identifier: CA1528949275
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871654_14871660delinsCTCAAGT , CM000667.2:g.14871654_14871660delinsCTCAAGT GRCh38
NC_000005.9:g.14871763_14871769delinsCTCAAGT , CM000667.1:g.14871763_14871769delinsCTCAAGT GRCh37
NC_000005.8:g.14924763_14924769delinsCTCAAGT NCBI36
NG_008273.1:g.5119_5125delinsACTTGAG
NG_008273.2:g.5126_5132delinsACTTGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-213_-207delinsACTTGAG MANE Select ENSP00000284268.6:n.-213_-207delinsACTTGAG
ENST00000284268.6:c.-213_-207delinsACTTGAG ENSP00000284268.6:n.-213_-207delinsACTTGAG
ENST00000505140.1:c.-213_-207delinsACTTGAG ENSP00000426332.1:n.-213_-207delinsACTTGAG
NM_054027.4:c.-213_-207delinsACTTGAG NP_473368.1:n.-213_-207delinsACTTGAG
XM_011514067.1:c.-213_-207delinsACTTGAG XP_011512369.1:n.-213_-207delinsACTTGAG
NM_054027.5:c.-213_-207delinsACTTGAG NP_473368.1:n.-213_-207delinsACTTGAG
NM_054027.6:c.-213_-207delinsACTTGAG MANE Select NP_473368.1:n.-213_-207delinsACTTGAG