Canonical Allele Identifier: CA1528949136
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871520_14871524delinsGGGGC , CM000667.2:g.14871520_14871524delinsGGGGC GRCh38
NC_000005.9:g.14871629_14871633delinsGGGGC , CM000667.1:g.14871629_14871633delinsGGGGC GRCh37
NC_000005.8:g.14924629_14924633delinsGGGGC NCBI36
NG_008273.1:g.5255_5259delinsGCCCC
NG_008273.2:g.5262_5266delinsGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-77_-73delinsGCCCC MANE Select ENSP00000284268.6:n.-77_-73delinsGCCCC
ENST00000284268.6:c.-77_-73delinsGCCCC ENSP00000284268.6:n.-77_-73delinsGCCCC
ENST00000505140.1:c.-77_-73delinsGCCCC ENSP00000426332.1:n.-77_-73delinsGCCCC
NM_054027.4:c.-77_-73delinsGCCCC NP_473368.1:n.-77_-73delinsGCCCC
XM_011514067.1:c.-77_-73delinsGCCCC XP_011512369.1:n.-77_-73delinsGCCCC
NM_054027.5:c.-77_-73delinsGCCCC NP_473368.1:n.-77_-73delinsGCCCC
NM_054027.6:c.-77_-73delinsGCCCC MANE Select NP_473368.1:n.-77_-73delinsGCCCC