Canonical Allele Identifier: CA1913586738

Gene: SLC16A9

Linked Data

• dbSNP Id: rs1840664762

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59707325_59707338del , CM000672.2:g.59707325_59707338del	GRCh38
NC_000010.10:g.61467083_61467096del , CM000672.1:g.61467083_61467096del	GRCh37
NC_000010.9:g.61137089_61137102del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+2145_-37+2158del MANE Select	ENSP00000378757.3:n.-37+2145_-37+2158del
ENST00000395347.1:c.-36-23007_-36-22994del	ENSP00000378756.1:n.-36-23007_-36-22994del
ENST00000395348.7:c.-37+2145_-37+2158del	ENSP00000378757.3:n.-37+2145_-37+2158del
ENST00000490066.1:n.222+1272_222+1285del
NM_194298.2:c.-37+2145_-37+2158del	NP_919274.1:n.-37+2145_-37+2158del
NM_001323977.1:c.-168+2678_-168+2691del	NP_001310906.1:n.-168+2678_-168+2691del
NM_001323978.1:c.-250-146_-250-133del	NP_001310907.1:n.-250-146_-250-133del
NM_001323979.1:c.-168+2375_-168+2388del	NP_001310908.1:n.-168+2375_-168+2388del
NM_001323980.1:c.-168+2145_-168+2158del	NP_001310909.1:n.-168+2145_-168+2158del
NM_001323981.1:c.-119-146_-119-133del	NP_001310910.1:n.-119-146_-119-133del
XM_017015883.1:c.-37+2145_-37+2158del	XP_016871372.1:n.-37+2145_-37+2158del
XM_017015884.2:c.-182+2145_-182+2158del	XP_016871373.1:n.-182+2145_-182+2158del
NM_001323978.2:c.-250-146_-250-133del	NP_001310907.1:n.-250-146_-250-133del
NM_001323979.2:c.-168+2375_-168+2388del	NP_001310908.1:n.-168+2375_-168+2388del
NM_001323980.2:c.-168+2145_-168+2158del	NP_001310909.1:n.-168+2145_-168+2158del
NM_001323981.2:c.-119-146_-119-133del	NP_001310910.1:n.-119-146_-119-133del
NM_194298.3:c.-37+2145_-37+2158del MANE Select	NP_919274.1:n.-37+2145_-37+2158del