Canonical Allele Identifier: CA1654828643

Gene: SLC16A10

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111223033T= , CM000668.2:g.111223033T=	GRCh38
NC_000006.11:g.111544236T= , CM000668.1:g.111544236T=	GRCh37
NC_000006.10:g.111650929T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*798T= MANE Select	ENSP00000357844.4:n.*798T=
ENST00000368850.4:c.*798T=	ENSP00000357843.1:n.*798T=
NM_018593.4:c.*798T=	NP_061063.2:n.*798T=
XM_017010237.1:c.*798T=	XP_016865726.1:n.*798T=
XR_001743158.1:n.2628T=
NM_018593.5:c.*798T= MANE Select	NP_061063.2:n.*798T=