Canonical Allele Identifier: CA1654828628

Gene: SLC16A10

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111222996A= , CM000668.2:g.111222996A=	GRCh38
NC_000006.11:g.111544199A= , CM000668.1:g.111544199A=	GRCh37
NC_000006.10:g.111650892A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*761A= MANE Select	ENSP00000357844.4:n.*761A=
ENST00000368850.4:c.*761A=	ENSP00000357843.1:n.*761A=
ENST00000368851.9:c.*761A=	ENSP00000357844.4:n.*761A=
NM_018593.4:c.*761A=	NP_061063.2:n.*761A=
XM_005266818.2:c.*715A=	XP_005266875.1:n.*715A=
XM_017010237.1:c.*761A=	XP_016865726.1:n.*761A=
XR_001743158.1:n.2591A=
NM_018593.5:c.*761A= MANE Select	NP_061063.2:n.*761A=