Canonical Allele Identifier: CA1528880789
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716764A= , CM000667.2:g.14716764A= GRCh38
NC_000005.9:g.14716873A= , CM000667.1:g.14716873A= GRCh37
NC_000005.8:g.14769873A= NCBI36
NG_008273.1:g.160015T=
NG_008273.2:g.160022T=
NG_051625.1:g.60971A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1083T= MANE Select ENSP00000284268.6:p.Phe361=
ENST00000284268.6:c.1083T= ENSP00000284268.6:p.Phe361=
ENST00000502585.1:n.325T=
NM_054027.4:c.1083T= NP_473368.1:p.Phe361=
NM_054027.5:c.1083T= NP_473368.1:p.Phe361=
XM_017009644.2:c.999T= XP_016865133.1:p.Phe333=
NM_054027.6:c.1083T= MANE Select NP_473368.1:p.Phe361=