Canonical Allele Identifier: CA2680016505

Gene: SLC16A10

Linked Data

• gnomAD v4: 6-111222998-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111223002del , CM000668.2:g.111223002del	GRCh38
NC_000006.11:g.111544205del , CM000668.1:g.111544205del	GRCh37
NC_000006.10:g.111650898del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*767del MANE Select	ENSP00000357844.4:n.*767del
ENST00000368850.4:c.*767del	ENSP00000357843.1:n.*767del
ENST00000368851.9:c.*767del	ENSP00000357844.4:n.*767del
NM_018593.4:c.*767del	NP_061063.2:n.*767del
XM_005266818.2:c.*721del	XP_005266875.1:n.*721del
XM_017010237.1:c.*767del	XP_016865726.1:n.*767del
XR_001743158.1:n.2597del
NM_018593.5:c.*767del MANE Select	NP_061063.2:n.*767del