Canonical Allele Identifier: CA1913586736

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59707321_59707336delinsAGGGAAGGGAAGGGAG , CM000672.2:g.59707321_59707336delinsAGGGAAGGGAAGGGAG	GRCh38
NC_000010.10:g.61467079_61467094delinsAGGGAAGGGAAGGGAG , CM000672.1:g.61467079_61467094delinsAGGGAAGGGAAGGGAG	GRCh37
NC_000010.9:g.61137085_61137100delinsAGGGAAGGGAAGGGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT MANE Select	ENSP00000378757.3:n.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT
ENST00000395347.1:c.-36-23009_-36-22994delinsCTCCCTTCCCTTCCCT	ENSP00000378756.1:n.-36-23009_-36-22994delinsCTCCCTTCCCTTCCCT...
ENST00000395348.7:c.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT	ENSP00000378757.3:n.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT
ENST00000490066.1:n.222+1270_222+1285delinsCTCCCTTCCCTTCCCT
NM_194298.2:c.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT	NP_919274.1:n.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT
NM_001323977.1:c.-168+2676_-168+2691delinsCTCCCTTCCCTTCCCT	NP_001310906.1:n.-168+2676_-168+2691delinsCTCCCTTCCCTTCCCT
NM_001323978.1:c.-250-148_-250-133delinsCTCCCTTCCCTTCCCT	NP_001310907.1:n.-250-148_-250-133delinsCTCCCTTCCCTTCCCT
NM_001323979.1:c.-168+2373_-168+2388delinsCTCCCTTCCCTTCCCT	NP_001310908.1:n.-168+2373_-168+2388delinsCTCCCTTCCCTTCCCT
NM_001323980.1:c.-168+2143_-168+2158delinsCTCCCTTCCCTTCCCT	NP_001310909.1:n.-168+2143_-168+2158delinsCTCCCTTCCCTTCCCT
NM_001323981.1:c.-119-148_-119-133delinsCTCCCTTCCCTTCCCT	NP_001310910.1:n.-119-148_-119-133delinsCTCCCTTCCCTTCCCT
XM_017015883.1:c.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT	XP_016871372.1:n.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT
XM_017015884.2:c.-182+2143_-182+2158delinsCTCCCTTCCCTTCCCT	XP_016871373.1:n.-182+2143_-182+2158delinsCTCCCTTCCCTTCCCT
NM_001323978.2:c.-250-148_-250-133delinsCTCCCTTCCCTTCCCT	NP_001310907.1:n.-250-148_-250-133delinsCTCCCTTCCCTTCCCT
NM_001323979.2:c.-168+2373_-168+2388delinsCTCCCTTCCCTTCCCT	NP_001310908.1:n.-168+2373_-168+2388delinsCTCCCTTCCCTTCCCT
NM_001323980.2:c.-168+2143_-168+2158delinsCTCCCTTCCCTTCCCT	NP_001310909.1:n.-168+2143_-168+2158delinsCTCCCTTCCCTTCCCT
NM_001323981.2:c.-119-148_-119-133delinsCTCCCTTCCCTTCCCT	NP_001310910.1:n.-119-148_-119-133delinsCTCCCTTCCCTTCCCT
NM_194298.3:c.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT MANE Select	NP_919274.1:n.-37+2143_-37+2158delinsCTCCCTTCCCTTCCCT