Canonical Allele Identifier: CA1654828638

Gene: SLC16A10

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111223023C= , CM000668.2:g.111223023C=	GRCh38
NC_000006.11:g.111544226C= , CM000668.1:g.111544226C=	GRCh37
NC_000006.10:g.111650919C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*788C= MANE Select	ENSP00000357844.4:n.*788C=
ENST00000368850.4:c.*788C=	ENSP00000357843.1:n.*788C=
NM_018593.4:c.*788C=	NP_061063.2:n.*788C=
XM_017010237.1:c.*788C=	XP_016865726.1:n.*788C=
XR_001743158.1:n.2618C=
NM_018593.5:c.*788C= MANE Select	NP_061063.2:n.*788C=