Canonical Allele Identifier: CA2001152699
Gene: ANKK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399652C= , CM000673.2:g.113399652C= GRCh38
NC_000011.9:g.113270374C= , CM000673.1:g.113270374C= GRCh37
NC_000011.8:g.112775584C= NCBI36
NG_012976.1:g.16862C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303941.4:c.1683C= MANE Select ENSP00000306678.3:p.Tyr561=
ENST00000303941.3:c.1683C= ENSP00000306678.3:p.Tyr561=
NM_178510.1:c.1683C= NP_848605.1:p.Tyr561=
XM_011542736.1:c.1716C= XP_011541038.1:p.Tyr572=
XM_011542737.1:c.1686C= XP_011541039.1:p.Tyr562=
XM_011542738.1:c.1494C= XP_011541040.1:p.Tyr498=
XM_011542736.2:c.1716C= XP_011541038.1:p.Tyr572=
XM_011542737.2:c.1686C= XP_011541039.1:p.Tyr562=
XM_011542738.2:c.1494C= XP_011541040.1:p.Tyr498=
XM_017017475.1:c.1713C= XP_016872964.1:p.Tyr571=
NM_178510.2:c.1683C= MANE Select NP_848605.1:p.Tyr561=