Canonical Allele Identifier: CA2788176289

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59707290_59707358del , CM000672.2:g.59707290_59707358del	GRCh38
NC_000010.10:g.61467048_61467116del , CM000672.1:g.61467048_61467116del	GRCh37
NC_000010.9:g.61137054_61137122del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+2123_-37+2191del MANE Select	ENSP00000378757.3:n.-37+2123_-37+2191del
ENST00000395347.1:c.-36-23029_-36-22961del	ENSP00000378756.1:n.-36-23029_-36-22961del
ENST00000395348.7:c.-37+2123_-37+2191del	ENSP00000378757.3:n.-37+2123_-37+2191del
ENST00000490066.1:n.222+1250_222+1318del
NM_194298.2:c.-37+2123_-37+2191del	NP_919274.1:n.-37+2123_-37+2191del
NM_001323977.1:c.-168+2656_-168+2724del	NP_001310906.1:n.-168+2656_-168+2724del
NM_001323978.1:c.-250-168_-250-100del	NP_001310907.1:n.-250-168_-250-100del
NM_001323979.1:c.-168+2353_-168+2421del	NP_001310908.1:n.-168+2353_-168+2421del
NM_001323980.1:c.-168+2123_-168+2191del	NP_001310909.1:n.-168+2123_-168+2191del
NM_001323981.1:c.-119-168_-119-100del	NP_001310910.1:n.-119-168_-119-100del
XM_017015883.1:c.-37+2123_-37+2191del	XP_016871372.1:n.-37+2123_-37+2191del
XM_017015884.2:c.-182+2123_-182+2191del	XP_016871373.1:n.-182+2123_-182+2191del
NM_001323978.2:c.-250-168_-250-100del	NP_001310907.1:n.-250-168_-250-100del
NM_001323979.2:c.-168+2353_-168+2421del	NP_001310908.1:n.-168+2353_-168+2421del
NM_001323980.2:c.-168+2123_-168+2191del	NP_001310909.1:n.-168+2123_-168+2191del
NM_001323981.2:c.-119-168_-119-100del	NP_001310910.1:n.-119-168_-119-100del
NM_194298.3:c.-37+2123_-37+2191del MANE Select	NP_919274.1:n.-37+2123_-37+2191del