Canonical Allele Identifier: CA2765371450
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716926dup , CM000667.2:g.14716926dup GRCh38
NC_000005.9:g.14717035dup , CM000667.1:g.14717035dup GRCh37
NC_000005.8:g.14770035dup NCBI36
NG_008273.1:g.159853dup
NG_008273.2:g.159860dup
NG_051625.1:g.61133dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1012-91dup MANE Select ENSP00000284268.6:n.1012-91dup
ENST00000284268.6:c.1012-91dup ENSP00000284268.6:n.1012-91dup
ENST00000502585.1:n.163dup
NM_054027.4:c.1012-91dup NP_473368.1:n.1012-91dup
NM_054027.5:c.1012-91dup NP_473368.1:n.1012-91dup
XM_017009644.2:c.928-91dup XP_016865133.1:n.928-91dup
NM_054027.6:c.1012-91dup MANE Select NP_473368.1:n.1012-91dup