Canonical Allele Identifier: CA1528904036
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14769215C= , CM000667.2:g.14769215C= GRCh38
NC_000005.9:g.14769324C= , CM000667.1:g.14769324C= GRCh37
NC_000005.8:g.14822324C= NCBI36
NG_008273.1:g.107564G=
NG_008273.2:g.107571G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.97-24G= MANE Select ENSP00000284268.6:n.97-24G=
ENST00000284268.6:c.97-24G= ENSP00000284268.6:n.97-24G=
ENST00000503389.1:n.103-24G=
ENST00000513115.1:n.122-24G=
NM_054027.4:c.97-24G= NP_473368.1:n.97-24G=
XM_011514067.1:c.97-24G= XP_011512369.1:n.97-24G=
NM_054027.5:c.97-24G= NP_473368.1:n.97-24G=
XM_017009644.2:c.13-24G= XP_016865133.1:n.13-24G=
NM_054027.6:c.97-24G= MANE Select NP_473368.1:n.97-24G=