Canonical Allele Identifier: CA2788176297

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59707325_59707326insCGGGA , CM000672.2:g.59707325_59707326insCGGGA	GRCh38
NC_000010.10:g.61467083_61467084insCGGGA , CM000672.1:g.61467083_61467084insCGGGA	GRCh37
NC_000010.9:g.61137089_61137090insCGGGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+2157_-37+2158insGTCCC MANE Select	ENSP00000378757.3:n.-37+2157_-37+2158insGTCCC
ENST00000395347.1:c.-36-22995_-36-22994insGTCCC	ENSP00000378756.1:n.-36-22995_-36-22994insGTCCC
ENST00000395348.7:c.-37+2157_-37+2158insGTCCC	ENSP00000378757.3:n.-37+2157_-37+2158insGTCCC
ENST00000490066.1:n.222+1284_222+1285insGTCCC
NM_194298.2:c.-37+2157_-37+2158insGTCCC	NP_919274.1:n.-37+2157_-37+2158insGTCCC
NM_001323977.1:c.-168+2690_-168+2691insGTCCC	NP_001310906.1:n.-168+2690_-168+2691insGTCCC
NM_001323978.1:c.-250-134_-250-133insGTCCC	NP_001310907.1:n.-250-134_-250-133insGTCCC
NM_001323979.1:c.-168+2387_-168+2388insGTCCC	NP_001310908.1:n.-168+2387_-168+2388insGTCCC
NM_001323980.1:c.-168+2157_-168+2158insGTCCC	NP_001310909.1:n.-168+2157_-168+2158insGTCCC
NM_001323981.1:c.-119-134_-119-133insGTCCC	NP_001310910.1:n.-119-134_-119-133insGTCCC
XM_017015883.1:c.-37+2157_-37+2158insGTCCC	XP_016871372.1:n.-37+2157_-37+2158insGTCCC
XM_017015884.2:c.-182+2157_-182+2158insGTCCC	XP_016871373.1:n.-182+2157_-182+2158insGTCCC
NM_001323978.2:c.-250-134_-250-133insGTCCC	NP_001310907.1:n.-250-134_-250-133insGTCCC
NM_001323979.2:c.-168+2387_-168+2388insGTCCC	NP_001310908.1:n.-168+2387_-168+2388insGTCCC
NM_001323980.2:c.-168+2157_-168+2158insGTCCC	NP_001310909.1:n.-168+2157_-168+2158insGTCCC
NM_001323981.2:c.-119-134_-119-133insGTCCC	NP_001310910.1:n.-119-134_-119-133insGTCCC
NM_194298.3:c.-37+2157_-37+2158insGTCCC MANE Select	NP_919274.1:n.-37+2157_-37+2158insGTCCC