Canonical Allele Identifier: CA477042547
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270059C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399337C>G , CM000673.2:g.113399337C>G GRCh38
NC_000011.9:g.113270059C>G , CM000673.1:g.113270059C>G GRCh37
NC_000011.8:g.112775269C>G NCBI36
NG_012976.1:g.16547C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303941.4:c.1368C>G MANE Select ENSP00000306678.3:p.Ala456=
ENST00000303941.3:c.1368C>G ENSP00000306678.3:p.Ala456=
NM_178510.1:c.1368C>G NP_848605.1:p.Ala456=
XM_011542736.1:c.1401C>G XP_011541038.1:p.Ala467=
XM_011542737.1:c.1371C>G XP_011541039.1:p.Ala457=
XM_011542738.1:c.1179C>G XP_011541040.1:p.Ala393=
XM_011542736.2:c.1401C>G XP_011541038.1:p.Ala467=
XM_011542737.2:c.1371C>G XP_011541039.1:p.Ala457=
XM_011542738.2:c.1179C>G XP_011541040.1:p.Ala393=
XM_017017475.1:c.1398C>G XP_016872964.1:p.Ala466=
NM_178510.2:c.1368C>G MANE Select NP_848605.1:p.Ala456=