Canonical Allele Identifier: CA1528880849
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716876G= , CM000667.2:g.14716876G= GRCh38
NC_000005.9:g.14716985G= , CM000667.1:g.14716985G= GRCh37
NC_000005.8:g.14769985G= NCBI36
NG_008273.1:g.159903C=
NG_008273.2:g.159910C=
NG_051625.1:g.61083G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1012-41C= MANE Select ENSP00000284268.6:n.1012-41C=
ENST00000284268.6:c.1012-41C= ENSP00000284268.6:n.1012-41C=
ENST00000502585.1:n.213C=
NM_054027.4:c.1012-41C= NP_473368.1:n.1012-41C=
NM_054027.5:c.1012-41C= NP_473368.1:n.1012-41C=
XM_017009644.2:c.928-41C= XP_016865133.1:n.928-41C=
NM_054027.6:c.1012-41C= MANE Select NP_473368.1:n.1012-41C=