Canonical Allele Identifier: CA917419686
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs1561093271

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871519del , CM000667.2:g.14871519del GRCh38
NC_000005.9:g.14871628del , CM000667.1:g.14871628del GRCh37
NC_000005.8:g.14924628del NCBI36
NG_008273.1:g.5260del
NG_008273.2:g.5267del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-72del MANE Select ENSP00000284268.6:n.-72del
ENST00000284268.6:c.-72del ENSP00000284268.6:n.-72del
ENST00000505140.1:c.-72del ENSP00000426332.1:n.-72del
NM_054027.4:c.-72del NP_473368.1:n.-72del
XM_011514067.1:c.-72del XP_011512369.1:n.-72del
NM_054027.5:c.-72del NP_473368.1:n.-72del
NM_054027.6:c.-72del MANE Select NP_473368.1:n.-72del