Canonical Allele Identifier: CA208159726

Gene: SLC16A9

Linked Data

• dbSNP Id: rs1052122048
• gnomAD v3: 10-59709271-AC-A
• gnomAD v4: 10-59709271-AC-A
• MyVariant Identifiers: chr10:g.61469030del (hg19) ; chr10:g.59709272del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59709275del , CM000672.2:g.59709275del	GRCh38
NC_000010.10:g.61469033del , CM000672.1:g.61469033del	GRCh37
NC_000010.9:g.61139039del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395348.8:c.-37+207del MANE Select	ENSP00000378757.3:n.-37+207del
ENST00000395347.1:c.-36-24945del	ENSP00000378756.1:n.-36-24945del
ENST00000395348.7:c.-37+207del	ENSP00000378757.3:n.-37+207del
ENST00000490066.1:n.44+207del
NM_194298.2:c.-37+207del	NP_919274.1:n.-37+207del
NM_001323977.1:c.-168+740del	NP_001310906.1:n.-168+740del
NM_001323978.1:c.-251+207del	NP_001310907.1:n.-251+207del
NM_001323979.1:c.-168+437del	NP_001310908.1:n.-168+437del
NM_001323980.1:c.-168+207del	NP_001310909.1:n.-168+207del
NM_001323981.1:c.-120+207del	NP_001310910.1:n.-120+207del
XM_017015883.1:c.-37+207del	XP_016871372.1:n.-37+207del
XM_017015884.2:c.-182+207del	XP_016871373.1:n.-182+207del
NM_001323978.2:c.-251+207del	NP_001310907.1:n.-251+207del
NM_001323979.2:c.-168+437del	NP_001310908.1:n.-168+437del
NM_001323980.2:c.-168+207del	NP_001310909.1:n.-168+207del
NM_001323981.2:c.-120+207del	NP_001310910.1:n.-120+207del
NM_194298.3:c.-37+207del MANE Select	NP_919274.1:n.-37+207del