Canonical Allele Identifier: CA2437509389

Gene: SLC16A2

Linked Data

• dbSNP Id: rs1930528897

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74529199_74529201del , CM000685.2:g.74529199_74529201del	GRCh38
NC_000023.10:g.73749034_73749036del , CM000685.1:g.73749034_73749036del	GRCh37
NC_000023.9:g.73665759_73665761del	NCBI36
NG_011641.1:g.112950_112952del
NG_011641.2:g.112950_112952del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.1171-14_1171-12del MANE Select	ENSP00000465734.1:n.1171-14_1171-12del
ENST00000636771.1:c.1080-14_1080-12del
ENST00000587091.5:c.1171-14_1171-12del	ENSP00000465734.1:n.1171-14_1171-12del
ENST00000590447.1:c.611-2134_611-2132del
NM_006517.4:c.1171-14_1171-12del	NP_006508.2:n.1171-14_1171-12del
XM_005262294.1:c.1171-2134_1171-2132del	XP_005262351.1:n.1171-2134_1171-2132del
NM_006517.5:c.1171-14_1171-12del MANE Select	NP_006508.2:n.1171-14_1171-12del