Canonical Allele Identifier: CA477043014
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270740A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113400018A>G , CM000673.2:g.113400018A>G GRCh38
NC_000011.9:g.113270740A>G , CM000673.1:g.113270740A>G GRCh37
NC_000011.8:g.112775950A>G NCBI36
NG_012976.1:g.17228A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303941.4:c.2049A>G MANE Select ENSP00000306678.3:p.Ala683=
ENST00000303941.3:c.2049A>G ENSP00000306678.3:p.Ala683=
NM_178510.1:c.2049A>G NP_848605.1:p.Ala683=
XM_011542736.1:c.2082A>G XP_011541038.1:p.Ala694=
XM_011542737.1:c.2052A>G XP_011541039.1:p.Ala684=
XM_011542738.1:c.1860A>G XP_011541040.1:p.Ala620=
XM_011542736.2:c.2082A>G XP_011541038.1:p.Ala694=
XM_011542737.2:c.2052A>G XP_011541039.1:p.Ala684=
XM_011542738.2:c.1860A>G XP_011541040.1:p.Ala620=
XM_017017475.1:c.2079A>G XP_016872964.1:p.Ala693=
NM_178510.2:c.2049A>G MANE Select NP_848605.1:p.Ala683=