Canonical Allele Identifier: CA1072525299

Gene: SLC6A3

Linked Data

• dbSNP Id: rs1756217115
• gnomAD v3: 5-1414469-G-GGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGGGAAGGCA
• gnomAD v4: 5-1414469-G-GGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGGGAAGGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1414469_1414470insGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGGGAAGGCA , CM000667.2:g.1414469_1414470insGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGGGAAGGCA	GRCh38
NC_000005.9:g.1414584_1414585insGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGGGAAGGCA , CM000667.1:g.1414584_1414585insGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGGGAAGGCA	GRCh37
NC_000005.8:g.1467584_1467585insGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCGGGAGGGTCAGGGCAGGGAAGGCA	NCBI36
NG_015885.1:g.35959_35960insTGCCTTCCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.1156+221_1156+222insTGCCTTCCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACC MANE Select	ENSP00000270349.9:n.1156+221_1156+222insTGCCTTCCCTGCCCTGACCCT...
ENST00000270349.11:c.1156+221_1156+222insTGCCTTCCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACC	ENSP00000270349.9:n.1156+221_1156+222insTGCCTTCCCTGCCCTGACCCT...
NM_001044.4:c.1156+221_1156+222insTGCCTTCCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACC	NP_001035.1:n.1156+221_1156+222insTGCCTTCCCTGCCCTGACCCTCCCGGC...
NM_001044.5:c.1156+221_1156+222insTGCCTTCCCTGCCCTGACCCTCCCGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACC MANE Select	NP_001035.1:n.1156+221_1156+222insTGCCTTCCCTGCCCTGACCCTCCCGGC...