Canonical Allele Identifier: CA1528903977
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14769070C= , CM000667.2:g.14769070C= GRCh38
NC_000005.9:g.14769179C= , CM000667.1:g.14769179C= GRCh37
NC_000005.8:g.14822179C= NCBI36
NG_008273.1:g.107709G=
NG_008273.2:g.107716G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.218G= MANE Select ENSP00000284268.6:p.Gly73=
ENST00000646501.1:c.81G=
ENST00000284268.6:c.218G= ENSP00000284268.6:p.Gly73=
ENST00000503389.1:n.224G=
ENST00000513115.1:n.243G=
NM_054027.4:c.218G= NP_473368.1:p.Gly73=
XM_011514067.1:c.218G= XP_011512369.1:p.Gly73=
NM_054027.5:c.218G= NP_473368.1:p.Gly73=
XM_017009644.2:c.134G= XP_016865133.1:p.Gly45=
NM_054027.6:c.218G= MANE Select NP_473368.1:p.Gly73=