Canonical Allele Identifier: CA477042594
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270086T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399364T>A , CM000673.2:g.113399364T>A GRCh38
NC_000011.9:g.113270086T>A , CM000673.1:g.113270086T>A GRCh37
NC_000011.8:g.112775296T>A NCBI36
NG_012976.1:g.16574T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303941.4:c.1395T>A MANE Select ENSP00000306678.3:p.Leu465=
ENST00000303941.3:c.1395T>A ENSP00000306678.3:p.Leu465=
NM_178510.1:c.1395T>A NP_848605.1:p.Leu465=
XM_011542736.1:c.1428T>A XP_011541038.1:p.Leu476=
XM_011542737.1:c.1398T>A XP_011541039.1:p.Leu466=
XM_011542738.1:c.1206T>A XP_011541040.1:p.Leu402=
XM_011542736.2:c.1428T>A XP_011541038.1:p.Leu476=
XM_011542737.2:c.1398T>A XP_011541039.1:p.Leu466=
XM_011542738.2:c.1206T>A XP_011541040.1:p.Leu402=
XM_017017475.1:c.1425T>A XP_016872964.1:p.Leu475=
NM_178510.2:c.1395T>A MANE Select NP_848605.1:p.Leu465=