Canonical Allele Identifier: CA1528949210
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs1735830846

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871572_14871588dup , CM000667.2:g.14871572_14871588dup GRCh38
NC_000005.9:g.14871681_14871697dup , CM000667.1:g.14871681_14871697dup GRCh37
NC_000005.8:g.14924681_14924697dup NCBI36
NG_008273.1:g.5192_5208dup
NG_008273.2:g.5199_5215dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-140_-124dup MANE Select ENSP00000284268.6:n.-140_-124dup
ENST00000284268.6:c.-140_-124dup ENSP00000284268.6:n.-140_-124dup
ENST00000505140.1:c.-140_-124dup ENSP00000426332.1:n.-140_-124dup
NM_054027.4:c.-140_-124dup NP_473368.1:n.-140_-124dup
XM_011514067.1:c.-140_-124dup XP_011512369.1:n.-140_-124dup
NM_054027.5:c.-140_-124dup NP_473368.1:n.-140_-124dup
NM_054027.6:c.-140_-124dup MANE Select NP_473368.1:n.-140_-124dup