Canonical Allele Identifier: CA2680016417

Gene: SLC16A10

Linked Data

• gnomAD v4: 6-111222750-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111222750T>C , CM000668.2:g.111222750T>C	GRCh38
NC_000006.11:g.111543953T>C , CM000668.1:g.111543953T>C	GRCh37
NC_000006.10:g.111650646T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368851.10:c.*515T>C MANE Select	ENSP00000357844.4:n.*515T>C
ENST00000368850.4:c.*515T>C	ENSP00000357843.1:n.*515T>C
ENST00000368851.9:c.*515T>C	ENSP00000357844.4:n.*515T>C
NM_018593.4:c.*515T>C	NP_061063.2:n.*515T>C
XM_005266818.2:c.*469T>C	XP_005266875.1:n.*469T>C
XM_017010237.1:c.*515T>C	XP_016865726.1:n.*515T>C
XR_001743158.1:n.2345T>C
NM_018593.5:c.*515T>C MANE Select	NP_061063.2:n.*515T>C