Canonical Allele Identifier: CA1913586720

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59707313_59707326delinsGGAAGGGAAGGGAA , CM000672.2:g.59707313_59707326delinsGGAAGGGAAGGGAA	GRCh38
NC_000010.10:g.61467071_61467084delinsGGAAGGGAAGGGAA , CM000672.1:g.61467071_61467084delinsGGAAGGGAAGGGAA	GRCh37
NC_000010.9:g.61137077_61137090delinsGGAAGGGAAGGGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+2153_-37+2166delinsTTCCCTTCCCTTCC MANE Select	ENSP00000378757.3:n.-37+2153_-37+2166delinsTTCCCTTCCCTTCC
ENST00000395347.1:c.-36-22999_-36-22986delinsTTCCCTTCCCTTCC	ENSP00000378756.1:n.-36-22999_-36-22986delinsTTCCCTTCCCTTCC
ENST00000395348.7:c.-37+2153_-37+2166delinsTTCCCTTCCCTTCC	ENSP00000378757.3:n.-37+2153_-37+2166delinsTTCCCTTCCCTTCC
ENST00000490066.1:n.222+1280_222+1293delinsTTCCCTTCCCTTCC
NM_194298.2:c.-37+2153_-37+2166delinsTTCCCTTCCCTTCC	NP_919274.1:n.-37+2153_-37+2166delinsTTCCCTTCCCTTCC
NM_001323977.1:c.-168+2686_-168+2699delinsTTCCCTTCCCTTCC	NP_001310906.1:n.-168+2686_-168+2699delinsTTCCCTTCCCTTCC
NM_001323978.1:c.-250-138_-250-125delinsTTCCCTTCCCTTCC	NP_001310907.1:n.-250-138_-250-125delinsTTCCCTTCCCTTCC
NM_001323979.1:c.-168+2383_-168+2396delinsTTCCCTTCCCTTCC	NP_001310908.1:n.-168+2383_-168+2396delinsTTCCCTTCCCTTCC
NM_001323980.1:c.-168+2153_-168+2166delinsTTCCCTTCCCTTCC	NP_001310909.1:n.-168+2153_-168+2166delinsTTCCCTTCCCTTCC
NM_001323981.1:c.-119-138_-119-125delinsTTCCCTTCCCTTCC	NP_001310910.1:n.-119-138_-119-125delinsTTCCCTTCCCTTCC
XM_017015883.1:c.-37+2153_-37+2166delinsTTCCCTTCCCTTCC	XP_016871372.1:n.-37+2153_-37+2166delinsTTCCCTTCCCTTCC
XM_017015884.2:c.-182+2153_-182+2166delinsTTCCCTTCCCTTCC	XP_016871373.1:n.-182+2153_-182+2166delinsTTCCCTTCCCTTCC
NM_001323978.2:c.-250-138_-250-125delinsTTCCCTTCCCTTCC	NP_001310907.1:n.-250-138_-250-125delinsTTCCCTTCCCTTCC
NM_001323979.2:c.-168+2383_-168+2396delinsTTCCCTTCCCTTCC	NP_001310908.1:n.-168+2383_-168+2396delinsTTCCCTTCCCTTCC
NM_001323980.2:c.-168+2153_-168+2166delinsTTCCCTTCCCTTCC	NP_001310909.1:n.-168+2153_-168+2166delinsTTCCCTTCCCTTCC
NM_001323981.2:c.-119-138_-119-125delinsTTCCCTTCCCTTCC	NP_001310910.1:n.-119-138_-119-125delinsTTCCCTTCCCTTCC
NM_194298.3:c.-37+2153_-37+2166delinsTTCCCTTCCCTTCC MANE Select	NP_919274.1:n.-37+2153_-37+2166delinsTTCCCTTCCCTTCC