Canonical Allele Identifier: CA477043009
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270728A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113400006A>C , CM000673.2:g.113400006A>C GRCh38
NC_000011.9:g.113270728A>C , CM000673.1:g.113270728A>C GRCh37
NC_000011.8:g.112775938A>C NCBI36
NG_012976.1:g.17216A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303941.4:c.2037A>C MANE Select ENSP00000306678.3:p.Leu679=
ENST00000303941.3:c.2037A>C ENSP00000306678.3:p.Leu679=
NM_178510.1:c.2037A>C NP_848605.1:p.Leu679=
XM_011542736.1:c.2070A>C XP_011541038.1:p.Leu690=
XM_011542737.1:c.2040A>C XP_011541039.1:p.Leu680=
XM_011542738.1:c.1848A>C XP_011541040.1:p.Leu616=
XM_011542736.2:c.2070A>C XP_011541038.1:p.Leu690=
XM_011542737.2:c.2040A>C XP_011541039.1:p.Leu680=
XM_011542738.2:c.1848A>C XP_011541040.1:p.Leu616=
XM_017017475.1:c.2067A>C XP_016872964.1:p.Leu689=
NM_178510.2:c.2037A>C MANE Select NP_848605.1:p.Leu679=