Canonical Allele Identifier: CA2673314725
Gene: ANKH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871515_14871523del , CM000667.2:g.14871515_14871523del GRCh38
NC_000005.9:g.14871624_14871632del , CM000667.1:g.14871624_14871632del GRCh37
NC_000005.8:g.14924624_14924632del NCBI36
NG_008273.1:g.5259_5267del
NG_008273.2:g.5266_5274del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-73_-65del MANE Select ENSP00000284268.6:n.-73_-65del
ENST00000284268.6:c.-73_-65del ENSP00000284268.6:n.-73_-65del
ENST00000505140.1:c.-73_-65del ENSP00000426332.1:n.-73_-65del
NM_054027.4:c.-73_-65del NP_473368.1:n.-73_-65del
XM_011514067.1:c.-73_-65del XP_011512369.1:n.-73_-65del
NM_054027.5:c.-73_-65del NP_473368.1:n.-73_-65del
NM_054027.6:c.-73_-65del MANE Select NP_473368.1:n.-73_-65del