Canonical Allele Identifier: CA1913586739
Gene: SLC16A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.59707322_59707331delinsGGGAAGGGAA , CM000672.2:g.59707322_59707331delinsGGGAAGGGAA GRCh38
NC_000010.10:g.61467080_61467089delinsGGGAAGGGAA , CM000672.1:g.61467080_61467089delinsGGGAAGGGAA GRCh37
NC_000010.9:g.61137086_61137095delinsGGGAAGGGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395348.8:c.-37+2148_-37+2157delinsTTCCCTTCCC MANE Select ENSP00000378757.3:n.-37+2148_-37+2157delinsTTCCCTTCCC
ENST00000395347.1:c.-36-23004_-36-22995delinsTTCCCTTCCC ENSP00000378756.1:n.-36-23004_-36-22995delinsTTCCCTTCCC
ENST00000395348.7:c.-37+2148_-37+2157delinsTTCCCTTCCC ENSP00000378757.3:n.-37+2148_-37+2157delinsTTCCCTTCCC
ENST00000490066.1:n.222+1275_222+1284delinsTTCCCTTCCC
NM_194298.2:c.-37+2148_-37+2157delinsTTCCCTTCCC NP_919274.1:n.-37+2148_-37+2157delinsTTCCCTTCCC
NM_001323977.1:c.-168+2681_-168+2690delinsTTCCCTTCCC NP_001310906.1:n.-168+2681_-168+2690delinsTTCCCTTCCC
NM_001323978.1:c.-250-143_-250-134delinsTTCCCTTCCC NP_001310907.1:n.-250-143_-250-134delinsTTCCCTTCCC
NM_001323979.1:c.-168+2378_-168+2387delinsTTCCCTTCCC NP_001310908.1:n.-168+2378_-168+2387delinsTTCCCTTCCC
NM_001323980.1:c.-168+2148_-168+2157delinsTTCCCTTCCC NP_001310909.1:n.-168+2148_-168+2157delinsTTCCCTTCCC
NM_001323981.1:c.-119-143_-119-134delinsTTCCCTTCCC NP_001310910.1:n.-119-143_-119-134delinsTTCCCTTCCC
XM_017015883.1:c.-37+2148_-37+2157delinsTTCCCTTCCC XP_016871372.1:n.-37+2148_-37+2157delinsTTCCCTTCCC
XM_017015884.2:c.-182+2148_-182+2157delinsTTCCCTTCCC XP_016871373.1:n.-182+2148_-182+2157delinsTTCCCTTCCC
NM_001323978.2:c.-250-143_-250-134delinsTTCCCTTCCC NP_001310907.1:n.-250-143_-250-134delinsTTCCCTTCCC
NM_001323979.2:c.-168+2378_-168+2387delinsTTCCCTTCCC NP_001310908.1:n.-168+2378_-168+2387delinsTTCCCTTCCC
NM_001323980.2:c.-168+2148_-168+2157delinsTTCCCTTCCC NP_001310909.1:n.-168+2148_-168+2157delinsTTCCCTTCCC
NM_001323981.2:c.-119-143_-119-134delinsTTCCCTTCCC NP_001310910.1:n.-119-143_-119-134delinsTTCCCTTCCC
NM_194298.3:c.-37+2148_-37+2157delinsTTCCCTTCCC MANE Select NP_919274.1:n.-37+2148_-37+2157delinsTTCCCTTCCC