Canonical Allele Identifier: CA1528949162
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871529_14871536delinsGGGCGAGC , CM000667.2:g.14871529_14871536delinsGGGCGAGC GRCh38
NC_000005.9:g.14871638_14871645delinsGGGCGAGC , CM000667.1:g.14871638_14871645delinsGGGCGAGC GRCh37
NC_000005.8:g.14924638_14924645delinsGGGCGAGC NCBI36
NG_008273.1:g.5243_5250delinsGCTCGCCC
NG_008273.2:g.5250_5257delinsGCTCGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-89_-82delinsGCTCGCCC MANE Select ENSP00000284268.6:n.-89_-82delinsGCTCGCCC
ENST00000284268.6:c.-89_-82delinsGCTCGCCC ENSP00000284268.6:n.-89_-82delinsGCTCGCCC
ENST00000505140.1:c.-89_-82delinsGCTCGCCC ENSP00000426332.1:n.-89_-82delinsGCTCGCCC
NM_054027.4:c.-89_-82delinsGCTCGCCC NP_473368.1:n.-89_-82delinsGCTCGCCC
XM_011514067.1:c.-89_-82delinsGCTCGCCC XP_011512369.1:n.-89_-82delinsGCTCGCCC
NM_054027.5:c.-89_-82delinsGCTCGCCC NP_473368.1:n.-89_-82delinsGCTCGCCC
NM_054027.6:c.-89_-82delinsGCTCGCCC MANE Select NP_473368.1:n.-89_-82delinsGCTCGCCC