Canonical Allele Identifier: CA477042380
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113269840C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399118C>A , CM000673.2:g.113399118C>A GRCh38
NC_000011.9:g.113269840C>A , CM000673.1:g.113269840C>A GRCh37
NC_000011.8:g.112775050C>A NCBI36
NG_012976.1:g.16328C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000303941.4:c.1149C>A MANE Select ENSP00000306678.3:p.Ala383=
ENST00000303941.3:c.1149C>A ENSP00000306678.3:p.Ala383=
NM_178510.1:c.1149C>A NP_848605.1:p.Ala383=
XM_011542736.1:c.1182C>A XP_011541038.1:p.Ala394=
XM_011542737.1:c.1152C>A XP_011541039.1:p.Ala384=
XM_011542738.1:c.960C>A XP_011541040.1:p.Ala320=
XM_011542736.2:c.1182C>A XP_011541038.1:p.Ala394=
XM_011542737.2:c.1152C>A XP_011541039.1:p.Ala384=
XM_011542738.2:c.960C>A XP_011541040.1:p.Ala320=
XM_017017475.1:c.1179C>A XP_016872964.1:p.Ala393=
NM_178510.2:c.1149C>A MANE Select NP_848605.1:p.Ala383=