Canonical Allele Identifier: CA2673314721
Gene: ANKH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871511del , CM000667.2:g.14871511del GRCh38
NC_000005.9:g.14871620del , CM000667.1:g.14871620del GRCh37
NC_000005.8:g.14924620del NCBI36
NG_008273.1:g.5268del
NG_008273.2:g.5275del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-64del MANE Select ENSP00000284268.6:n.-64del
ENST00000284268.6:c.-64del ENSP00000284268.6:n.-64del
ENST00000505140.1:c.-64del ENSP00000426332.1:n.-64del
NM_054027.4:c.-64del NP_473368.1:n.-64del
XM_011514067.1:c.-64del XP_011512369.1:n.-64del
NM_054027.5:c.-64del NP_473368.1:n.-64del
NM_054027.6:c.-64del MANE Select NP_473368.1:n.-64del