Canonical Allele Identifier: CA477043020
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270752C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113400030C>T , CM000673.2:g.113400030C>T GRCh38
NC_000011.9:g.113270752C>T , CM000673.1:g.113270752C>T GRCh37
NC_000011.8:g.112775962C>T NCBI36
NG_012976.1:g.17240C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303941.4:c.2061C>T MANE Select ENSP00000306678.3:p.Ala687=
ENST00000303941.3:c.2061C>T ENSP00000306678.3:p.Ala687=
NM_178510.1:c.2061C>T NP_848605.1:p.Ala687=
XM_011542736.1:c.2094C>T XP_011541038.1:p.Ala698=
XM_011542737.1:c.2064C>T XP_011541039.1:p.Ala688=
XM_011542738.1:c.1872C>T XP_011541040.1:p.Ala624=
XM_011542736.2:c.2094C>T XP_011541038.1:p.Ala698=
XM_011542737.2:c.2064C>T XP_011541039.1:p.Ala688=
XM_011542738.2:c.1872C>T XP_011541040.1:p.Ala624=
XM_017017475.1:c.2091C>T XP_016872964.1:p.Ala697=
NM_178510.2:c.2061C>T MANE Select NP_848605.1:p.Ala687=