Canonical Allele Identifier: CA477042482
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270020T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399298T>G , CM000673.2:g.113399298T>G GRCh38
NC_000011.9:g.113270020T>G , CM000673.1:g.113270020T>G GRCh37
NC_000011.8:g.112775230T>G NCBI36
NG_012976.1:g.16508T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303941.4:c.1329T>G MANE Select ENSP00000306678.3:p.Thr443=
ENST00000303941.3:c.1329T>G ENSP00000306678.3:p.Thr443=
NM_178510.1:c.1329T>G NP_848605.1:p.Thr443=
XM_011542736.1:c.1362T>G XP_011541038.1:p.Thr454=
XM_011542737.1:c.1332T>G XP_011541039.1:p.Thr444=
XM_011542738.1:c.1140T>G XP_011541040.1:p.Thr380=
XM_011542736.2:c.1362T>G XP_011541038.1:p.Thr454=
XM_011542737.2:c.1332T>G XP_011541039.1:p.Thr444=
XM_011542738.2:c.1140T>G XP_011541040.1:p.Thr380=
XM_017017475.1:c.1359T>G XP_016872964.1:p.Thr453=
NM_178510.2:c.1329T>G MANE Select NP_848605.1:p.Thr443=