Canonical Allele Identifier: CA1654828642

Gene: SLC16A10

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111223032G= , CM000668.2:g.111223032G=	GRCh38
NC_000006.11:g.111544235G= , CM000668.1:g.111544235G=	GRCh37
NC_000006.10:g.111650928G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*797G= MANE Select	ENSP00000357844.4:n.*797G=
ENST00000368850.4:c.*797G=	ENSP00000357843.1:n.*797G=
NM_018593.4:c.*797G=	NP_061063.2:n.*797G=
XM_017010237.1:c.*797G=	XP_016865726.1:n.*797G=
XR_001743158.1:n.2627G=
NM_018593.5:c.*797G= MANE Select	NP_061063.2:n.*797G=