Canonical Allele Identifier: CA331283898

Gene: SLC16A2

Linked Data

• dbSNP Id: rs35146863

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74525669dup , CM000685.2:g.74525669dup	GRCh38
NC_000023.10:g.73745504dup , CM000685.1:g.73745504dup	GRCh37
NC_000023.9:g.73662229dup	NCBI36
NG_011641.1:g.109420dup
NG_011641.2:g.109420dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000587091.6:c.1027-81dup MANE Select	ENSP00000465734.1:n.1027-81dup
ENST00000636771.1:c.936-81dup
ENST00000587091.5:c.1027-81dup	ENSP00000465734.1:n.1027-81dup
ENST00000590447.1:c.467-81dup
NM_006517.4:c.1027-81dup	NP_006508.2:n.1027-81dup
XM_005262294.1:c.1027-81dup	XP_005262351.1:n.1027-81dup
XM_011531015.1:c.*31-81dup	XP_011529317.1:n.*31-81dup
NM_006517.5:c.1027-81dup MANE Select	NP_006508.2:n.1027-81dup