Canonical Allele Identifier: CA1528949219
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871582_14871601delinsGGCGGCGGCGGCTCCTCCTC , CM000667.2:g.14871582_14871601delinsGGCGGCGGCGGCTCCTCCTC GRCh38
NC_000005.9:g.14871691_14871710delinsGGCGGCGGCGGCTCCTCCTC , CM000667.1:g.14871691_14871710delinsGGCGGCGGCGGCTCCTCCTC GRCh37
NC_000005.8:g.14924691_14924710delinsGGCGGCGGCGGCTCCTCCTC NCBI36
NG_008273.1:g.5178_5197delinsGAGGAGGAGCCGCCGCCGCC
NG_008273.2:g.5185_5204delinsGAGGAGGAGCCGCCGCCGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-154_-135delinsGAGGAGGAGCCGCCGCCGCC MANE Select ENSP00000284268.6:n.-154_-135delinsGAGGAGGAGCCGCCGCCGCC
ENST00000284268.6:c.-154_-135delinsGAGGAGGAGCCGCCGCCGCC ENSP00000284268.6:n.-154_-135delinsGAGGAGGAGCCGCCGCCGCC
ENST00000505140.1:c.-154_-135delinsGAGGAGGAGCCGCCGCCGCC ENSP00000426332.1:n.-154_-135delinsGAGGAGGAGCCGCCGCCGCC
NM_054027.4:c.-154_-135delinsGAGGAGGAGCCGCCGCCGCC NP_473368.1:n.-154_-135delinsGAGGAGGAGCCGCCGCCGCC
XM_011514067.1:c.-154_-135delinsGAGGAGGAGCCGCCGCCGCC XP_011512369.1:n.-154_-135delinsGAGGAGGAGCCGCCGCCGCC
NM_054027.5:c.-154_-135delinsGAGGAGGAGCCGCCGCCGCC NP_473368.1:n.-154_-135delinsGAGGAGGAGCCGCCGCCGCC
NM_054027.6:c.-154_-135delinsGAGGAGGAGCCGCCGCCGCC MANE Select NP_473368.1:n.-154_-135delinsGAGGAGGAGCCGCCGCCGCC