Canonical Allele Identifier: CA1528880791
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716771A= , CM000667.2:g.14716771A= GRCh38
NC_000005.9:g.14716880A= , CM000667.1:g.14716880A= GRCh37
NC_000005.8:g.14769880A= NCBI36
NG_008273.1:g.160008T=
NG_008273.2:g.160015T=
NG_051625.1:g.60978A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1076T= MANE Select ENSP00000284268.6:p.Val359=
ENST00000284268.6:c.1076T= ENSP00000284268.6:p.Val359=
ENST00000502585.1:n.318T=
NM_054027.4:c.1076T= NP_473368.1:p.Val359=
NM_054027.5:c.1076T= NP_473368.1:p.Val359=
XM_017009644.2:c.992T= XP_016865133.1:p.Val331=
NM_054027.6:c.1076T= MANE Select NP_473368.1:p.Val359=