Canonical Allele Identifier: CA477042501
Gene: ANKK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.113270029G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113399307G>C , CM000673.2:g.113399307G>C GRCh38
NC_000011.9:g.113270029G>C , CM000673.1:g.113270029G>C GRCh37
NC_000011.8:g.112775239G>C NCBI36
NG_012976.1:g.16517G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303941.4:c.1338G>C MANE Select ENSP00000306678.3:p.Leu446=
ENST00000303941.3:c.1338G>C ENSP00000306678.3:p.Leu446=
NM_178510.1:c.1338G>C NP_848605.1:p.Leu446=
XM_011542736.1:c.1371G>C XP_011541038.1:p.Leu457=
XM_011542737.1:c.1341G>C XP_011541039.1:p.Leu447=
XM_011542738.1:c.1149G>C XP_011541040.1:p.Leu383=
XM_011542736.2:c.1371G>C XP_011541038.1:p.Leu457=
XM_011542737.2:c.1341G>C XP_011541039.1:p.Leu447=
XM_011542738.2:c.1149G>C XP_011541040.1:p.Leu383=
XM_017017475.1:c.1368G>C XP_016872964.1:p.Leu456=
NM_178510.2:c.1338G>C MANE Select NP_848605.1:p.Leu446=