Canonical Allele Identifier: CA1913586710
Gene: SLC16A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.59707306_59707336delinsAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAG , CM000672.2:g.59707306_59707336delinsAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAG GRCh38
NC_000010.10:g.61467064_61467094delinsAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAG , CM000672.1:g.61467064_61467094delinsAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAG GRCh37
NC_000010.9:g.61137070_61137100delinsAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395348.8:c.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT MANE Select ENSP00000378757.3:n.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTC...
ENST00000395347.1:c.-36-23009_-36-22979delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT ENSP00000378756.1:n.-36-23009_-36-22979delinsCTCCCTTCCCTTCCCT...
ENST00000395348.7:c.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT ENSP00000378757.3:n.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTC...
ENST00000490066.1:n.222+1270_222+1300delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT
NM_194298.2:c.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_919274.1:n.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTCCCTTCC...
NM_001323977.1:c.-168+2676_-168+2706delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310906.1:n.-168+2676_-168+2706delinsCTCCCTTCCCTTCCCTTCC...
NM_001323978.1:c.-250-148_-250-118delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310907.1:n.-250-148_-250-118delinsCTCCCTTCCCTTCCCTTCCCT...
NM_001323979.1:c.-168+2373_-168+2403delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310908.1:n.-168+2373_-168+2403delinsCTCCCTTCCCTTCCCTTCC...
NM_001323980.1:c.-168+2143_-168+2173delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310909.1:n.-168+2143_-168+2173delinsCTCCCTTCCCTTCCCTTCC...
NM_001323981.1:c.-119-148_-119-118delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310910.1:n.-119-148_-119-118delinsCTCCCTTCCCTTCCCTTCCCT...
XM_017015883.1:c.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT XP_016871372.1:n.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTCCCT...
XM_017015884.2:c.-182+2143_-182+2173delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT XP_016871373.1:n.-182+2143_-182+2173delinsCTCCCTTCCCTTCCCTTCC...
NM_001323978.2:c.-250-148_-250-118delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310907.1:n.-250-148_-250-118delinsCTCCCTTCCCTTCCCTTCCCT...
NM_001323979.2:c.-168+2373_-168+2403delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310908.1:n.-168+2373_-168+2403delinsCTCCCTTCCCTTCCCTTCC...
NM_001323980.2:c.-168+2143_-168+2173delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310909.1:n.-168+2143_-168+2173delinsCTCCCTTCCCTTCCCTTCC...
NM_001323981.2:c.-119-148_-119-118delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT NP_001310910.1:n.-119-148_-119-118delinsCTCCCTTCCCTTCCCTTCCCT...
NM_194298.3:c.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTCCCTTCCCTTCCCT MANE Select NP_919274.1:n.-37+2143_-37+2173delinsCTCCCTTCCCTTCCCTTCCCTTCC...