Canonical Allele Identifier: CA1654828636

Gene: SLC16A10

Linked Data

• dbSNP Id: rs1770932928

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111223018A>C , CM000668.2:g.111223018A>C	GRCh38
NC_000006.11:g.111544221A>C , CM000668.1:g.111544221A>C	GRCh37
NC_000006.10:g.111650914A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*783A>C MANE Select	ENSP00000357844.4:n.*783A>C
ENST00000368850.4:c.*783A>C	ENSP00000357843.1:n.*783A>C
ENST00000368851.9:c.*783A>C	ENSP00000357844.4:n.*783A>C
NM_018593.4:c.*783A>C	NP_061063.2:n.*783A>C
XM_005266818.2:c.*737A>C	XP_005266875.1:n.*737A>C
XM_017010237.1:c.*783A>C	XP_016865726.1:n.*783A>C
XR_001743158.1:n.2613A>C
NM_018593.5:c.*783A>C MANE Select	NP_061063.2:n.*783A>C