Canonical Allele Identifier: CA1072522242
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756205973

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414404_1414405insCCTGGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGG , CM000667.2:g.1414404_1414405insCCTGGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGG GRCh38
NC_000005.9:g.1414519_1414520insCCTGGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGG , CM000667.1:g.1414519_1414520insCCTGGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGG GRCh37
NC_000005.8:g.1467519_1467520insCCTGGAGGCACAAGGCAGGAAAGGCACTGGGTGGGGG NCBI36
NG_015885.1:g.36029_36030insACCCAGTGCCTTTCCTGCCTTGTGCCTCCAGGCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+291_1156+292insACCCAGTGCCTTTCCTGCCTTGTGCCTCCAGGCCCCC MANE Select ENSP00000270349.9:n.1156+291_1156+292insACCCAGTGCCTTTCCTGCCTT...
ENST00000270349.11:c.1156+291_1156+292insACCCAGTGCCTTTCCTGCCTTGTGCCTCCAGGCCCCC ENSP00000270349.9:n.1156+291_1156+292insACCCAGTGCCTTTCCTGCCTT...
NM_001044.4:c.1156+291_1156+292insACCCAGTGCCTTTCCTGCCTTGTGCCTCCAGGCCCCC NP_001035.1:n.1156+291_1156+292insACCCAGTGCCTTTCCTGCCTTGTGCCT...
NM_001044.5:c.1156+291_1156+292insACCCAGTGCCTTTCCTGCCTTGTGCCTCCAGGCCCCC MANE Select NP_001035.1:n.1156+291_1156+292insACCCAGTGCCTTTCCTGCCTTGTGCCT...