Canonical Allele Identifier: CA208157530
Gene: SLC16A9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.59689806A>G , CM000672.2:g.59689806A>G GRCh38
NC_000010.10:g.61449564A>G , CM000672.1:g.61449564A>G GRCh37
NC_000010.9:g.61119570A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395348.8:c.-36-5479T>C MANE Select ENSP00000378757.3:n.-36-5479T>C
ENST00000395347.1:c.-36-5479T>C ENSP00000378756.1:n.-36-5479T>C
ENST00000395348.7:c.-36-5479T>C ENSP00000378757.3:n.-36-5479T>C
ENST00000490066.1:n.223-5479T>C
NM_194298.2:c.-36-5479T>C NP_919274.1:n.-36-5479T>C
XM_011539488.1:c.-36-5479T>C XP_011537790.1:n.-36-5479T>C
NM_001323977.1:c.-167-5609T>C NP_001310906.1:n.-167-5609T>C
NM_001323978.1:c.-167-5609T>C NP_001310907.1:n.-167-5609T>C
NM_001323979.1:c.-167-5609T>C NP_001310908.1:n.-167-5609T>C
NM_001323980.1:c.-167-5609T>C NP_001310909.1:n.-167-5609T>C
NM_001323981.1:c.-36-5479T>C NP_001310910.1:n.-36-5479T>C
XM_017015883.1:c.-36-5479T>C XP_016871372.1:n.-36-5479T>C
XM_017015884.2:c.-37+2865T>C XP_016871373.1:n.-37+2865T>C
NM_001323978.2:c.-167-5609T>C NP_001310907.1:n.-167-5609T>C
NM_001323979.2:c.-167-5609T>C NP_001310908.1:n.-167-5609T>C
NM_001323980.2:c.-167-5609T>C NP_001310909.1:n.-167-5609T>C
NM_001323981.2:c.-36-5479T>C NP_001310910.1:n.-36-5479T>C
NM_194298.3:c.-36-5479T>C MANE Select NP_919274.1:n.-36-5479T>C
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