Canonical Allele Identifier: CA1528949137
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871521_14871524delinsGGGC , CM000667.2:g.14871521_14871524delinsGGGC GRCh38
NC_000005.9:g.14871630_14871633delinsGGGC , CM000667.1:g.14871630_14871633delinsGGGC GRCh37
NC_000005.8:g.14924630_14924633delinsGGGC NCBI36
NG_008273.1:g.5255_5258delinsGCCC
NG_008273.2:g.5262_5265delinsGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-77_-74delinsGCCC MANE Select ENSP00000284268.6:n.-77_-74delinsGCCC
ENST00000284268.6:c.-77_-74delinsGCCC ENSP00000284268.6:n.-77_-74delinsGCCC
ENST00000505140.1:c.-77_-74delinsGCCC ENSP00000426332.1:n.-77_-74delinsGCCC
NM_054027.4:c.-77_-74delinsGCCC NP_473368.1:n.-77_-74delinsGCCC
XM_011514067.1:c.-77_-74delinsGCCC XP_011512369.1:n.-77_-74delinsGCCC
NM_054027.5:c.-77_-74delinsGCCC NP_473368.1:n.-77_-74delinsGCCC
NM_054027.6:c.-77_-74delinsGCCC MANE Select NP_473368.1:n.-77_-74delinsGCCC