Canonical Allele Identifier: CA2788176281

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59707267_59707340del , CM000672.2:g.59707267_59707340del	GRCh38
NC_000010.10:g.61467025_61467098del , CM000672.1:g.61467025_61467098del	GRCh37
NC_000010.9:g.61137031_61137104del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+2147_-37+2220del MANE Select	ENSP00000378757.3:n.-37+2147_-37+2220del
ENST00000395347.1:c.-36-23005_-36-22932del	ENSP00000378756.1:n.-36-23005_-36-22932del
ENST00000395348.7:c.-37+2147_-37+2220del	ENSP00000378757.3:n.-37+2147_-37+2220del
ENST00000490066.1:n.222+1274_222+1347del
NM_194298.2:c.-37+2147_-37+2220del	NP_919274.1:n.-37+2147_-37+2220del
NM_001323977.1:c.-168+2680_-168+2753del	NP_001310906.1:n.-168+2680_-168+2753del
NM_001323978.1:c.-250-144_-250-71del	NP_001310907.1:n.-250-144_-250-71del
NM_001323979.1:c.-168+2377_-168+2450del	NP_001310908.1:n.-168+2377_-168+2450del
NM_001323980.1:c.-168+2147_-168+2220del	NP_001310909.1:n.-168+2147_-168+2220del
NM_001323981.1:c.-119-144_-119-71del	NP_001310910.1:n.-119-144_-119-71del
XM_017015883.1:c.-37+2147_-37+2220del	XP_016871372.1:n.-37+2147_-37+2220del
XM_017015884.2:c.-182+2147_-182+2220del	XP_016871373.1:n.-182+2147_-182+2220del
NM_001323978.2:c.-250-144_-250-71del	NP_001310907.1:n.-250-144_-250-71del
NM_001323979.2:c.-168+2377_-168+2450del	NP_001310908.1:n.-168+2377_-168+2450del
NM_001323980.2:c.-168+2147_-168+2220del	NP_001310909.1:n.-168+2147_-168+2220del
NM_001323981.2:c.-119-144_-119-71del	NP_001310910.1:n.-119-144_-119-71del
NM_194298.3:c.-37+2147_-37+2220del MANE Select	NP_919274.1:n.-37+2147_-37+2220del