Canonical Allele Identifier: CA1528903997
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14769150G= , CM000667.2:g.14769150G= GRCh38
NC_000005.9:g.14769259G= , CM000667.1:g.14769259G= GRCh37
NC_000005.8:g.14822259G= NCBI36
NG_008273.1:g.107629C=
NG_008273.2:g.107636C=

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.138C= MANE Select ENSP00000284268.6:p.Val46=
ENST00000646501.1:c.1C=
ENST00000284268.6:c.138C= ENSP00000284268.6:p.Val46=
ENST00000503389.1:n.144C=
ENST00000513115.1:n.163C=
NM_054027.4:c.138C= NP_473368.1:p.Val46=
XM_011514067.1:c.138C= XP_011512369.1:p.Val46=
NM_054027.5:c.138C= NP_473368.1:p.Val46=
XM_017009644.2:c.54C= XP_016865133.1:p.Val18=
NM_054027.6:c.138C= MANE Select NP_473368.1:p.Val46=