Canonical Allele Identifier: CA1528949142
Gene: ANKH HGNC NCBI

Linked Data

dbSNP Id: rs1735826424

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871525_14871533dup , CM000667.2:g.14871525_14871533dup GRCh38
NC_000005.9:g.14871634_14871642dup , CM000667.1:g.14871634_14871642dup GRCh37
NC_000005.8:g.14924634_14924642dup NCBI36
NG_008273.1:g.5246_5254dup
NG_008273.2:g.5253_5261dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-86_-78dup MANE Select ENSP00000284268.6:n.-86_-78dup
ENST00000284268.6:c.-86_-78dup ENSP00000284268.6:n.-86_-78dup
ENST00000505140.1:c.-86_-78dup ENSP00000426332.1:n.-86_-78dup
NM_054027.4:c.-86_-78dup NP_473368.1:n.-86_-78dup
XM_011514067.1:c.-86_-78dup XP_011512369.1:n.-86_-78dup
NM_054027.5:c.-86_-78dup NP_473368.1:n.-86_-78dup
NM_054027.6:c.-86_-78dup MANE Select NP_473368.1:n.-86_-78dup