Canonical Allele Identifier: CA1654828492

Gene: SLC16A10

Linked Data

• dbSNP Id: rs1430037682

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111222655T>G , CM000668.2:g.111222655T>G	GRCh38
NC_000006.11:g.111543858T>G , CM000668.1:g.111543858T>G	GRCh37
NC_000006.10:g.111650551T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*420T>G MANE Select	ENSP00000357844.4:n.*420T>G
ENST00000368850.4:c.*420T>G	ENSP00000357843.1:n.*420T>G
ENST00000368851.9:c.*420T>G	ENSP00000357844.4:n.*420T>G
NM_018593.4:c.*420T>G	NP_061063.2:n.*420T>G
XM_005266818.2:c.*374T>G	XP_005266875.1:n.*374T>G
XM_017010237.1:c.*420T>G	XP_016865726.1:n.*420T>G
XR_001743158.1:n.2250T>G
NM_018593.5:c.*420T>G MANE Select	NP_061063.2:n.*420T>G