Canonical Allele Identifier: CA2680016503

Gene: SLC16A10

Linked Data

• gnomAD v4: 6-111222990-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111222992del , CM000668.2:g.111222992del	GRCh38
NC_000006.11:g.111544195del , CM000668.1:g.111544195del	GRCh37
NC_000006.10:g.111650888del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368851.10:c.*757del MANE Select	ENSP00000357844.4:n.*757del
ENST00000368850.4:c.*757del	ENSP00000357843.1:n.*757del
ENST00000368851.9:c.*757del	ENSP00000357844.4:n.*757del
NM_018593.4:c.*757del	NP_061063.2:n.*757del
XM_005266818.2:c.*711del	XP_005266875.1:n.*711del
XM_017010237.1:c.*757del	XP_016865726.1:n.*757del
XR_001743158.1:n.2587del
NM_018593.5:c.*757del MANE Select	NP_061063.2:n.*757del