Canonical Allele Identifier: CA145250732

Gene: SLC16A10

Linked Data

• dbSNP Id: rs888510290
• MyVariant Identifiers: chr6:g.111544036C>T (hg19) ; chr6:g.111222833C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111222833C>T , CM000668.2:g.111222833C>T	GRCh38
NC_000006.11:g.111544036C>T , CM000668.1:g.111544036C>T	GRCh37
NC_000006.10:g.111650729C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*598C>T MANE Select	ENSP00000357844.4:n.*598C>T
ENST00000368850.4:c.*598C>T	ENSP00000357843.1:n.*598C>T
ENST00000368851.9:c.*598C>T	ENSP00000357844.4:n.*598C>T
NM_018593.4:c.*598C>T	NP_061063.2:n.*598C>T
XM_005266818.2:c.*552C>T	XP_005266875.1:n.*552C>T
XM_017010237.1:c.*598C>T	XP_016865726.1:n.*598C>T
XR_001743158.1:n.2428C>T
NM_018593.5:c.*598C>T MANE Select	NP_061063.2:n.*598C>T