Canonical Allele Identifier: CA1528904010
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14769175A= , CM000667.2:g.14769175A= GRCh38
NC_000005.9:g.14769284A= , CM000667.1:g.14769284A= GRCh37
NC_000005.8:g.14822284A= NCBI36
NG_008273.1:g.107604T=
NG_008273.2:g.107611T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.113T= MANE Select ENSP00000284268.6:p.Ile38=
ENST00000284268.6:c.113T= ENSP00000284268.6:p.Ile38=
ENST00000503389.1:n.119T=
ENST00000513115.1:n.138T=
NM_054027.4:c.113T= NP_473368.1:p.Ile38=
XM_011514067.1:c.113T= XP_011512369.1:p.Ile38=
NM_054027.5:c.113T= NP_473368.1:p.Ile38=
XM_017009644.2:c.29T= XP_016865133.1:p.Ile10=
NM_054027.6:c.113T= MANE Select NP_473368.1:p.Ile38=