Canonical Allele Identifier: CA1528880913
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716999C= , CM000667.2:g.14716999C= GRCh38
NC_000005.9:g.14717108C= , CM000667.1:g.14717108C= GRCh37
NC_000005.8:g.14770108C= NCBI36
NG_008273.1:g.159780G=
NG_008273.2:g.159787G=
NG_051625.1:g.61206C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1012-164G= MANE Select ENSP00000284268.6:n.1012-164G=
ENST00000284268.6:c.1012-164G= ENSP00000284268.6:n.1012-164G=
ENST00000502585.1:n.90G=
NM_054027.4:c.1012-164G= NP_473368.1:n.1012-164G=
NM_054027.5:c.1012-164G= NP_473368.1:n.1012-164G=
XM_017009644.2:c.928-164G= XP_016865133.1:n.928-164G=
NM_054027.6:c.1012-164G= MANE Select NP_473368.1:n.1012-164G=