Canonical Allele Identifier: CA1528880808
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716807T= , CM000667.2:g.14716807T= GRCh38
NC_000005.9:g.14716916T= , CM000667.1:g.14716916T= GRCh37
NC_000005.8:g.14769916T= NCBI36
NG_008273.1:g.159972A=
NG_008273.2:g.159979A=
NG_051625.1:g.61014T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1040A= MANE Select ENSP00000284268.6:p.Asn347=
ENST00000284268.6:c.1040A= ENSP00000284268.6:p.Asn347=
ENST00000502585.1:n.282A=
NM_054027.4:c.1040A= NP_473368.1:p.Asn347=
NM_054027.5:c.1040A= NP_473368.1:p.Asn347=
XM_017009644.2:c.956A= XP_016865133.1:p.Asn319=
NM_054027.6:c.1040A= MANE Select NP_473368.1:p.Asn347=