Canonical Allele Identifier: CA477042940
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270629G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399907G>C , CM000673.2:g.113399907G>C GRCh38
NC_000011.9:g.113270629G>C , CM000673.1:g.113270629G>C GRCh37
NC_000011.8:g.112775839G>C NCBI36
NG_012976.1:g.17117G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000303941.4:c.1938G>C MANE Select ENSP00000306678.3:p.Leu646=
ENST00000303941.3:c.1938G>C ENSP00000306678.3:p.Leu646=
NM_178510.1:c.1938G>C NP_848605.1:p.Leu646=
XM_011542736.1:c.1971G>C XP_011541038.1:p.Leu657=
XM_011542737.1:c.1941G>C XP_011541039.1:p.Leu647=
XM_011542738.1:c.1749G>C XP_011541040.1:p.Leu583=
XM_011542736.2:c.1971G>C XP_011541038.1:p.Leu657=
XM_011542737.2:c.1941G>C XP_011541039.1:p.Leu647=
XM_011542738.2:c.1749G>C XP_011541040.1:p.Leu583=
XM_017017475.1:c.1968G>C XP_016872964.1:p.Leu656=
NM_178510.2:c.1938G>C MANE Select NP_848605.1:p.Leu646=