Canonical Allele Identifier: CA1072526594

Gene: SLC6A3

Linked Data

• gnomAD v3: 5-1414491-T-TCAGGGCAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGGGCCGGGAGGGG
• gnomAD v4: 5-1414491-T-TCAGGGCAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGGGCCGGGAGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1414497_1414498insAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGC , CM000667.2:g.1414497_1414498insAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGC	GRCh38
NC_000005.9:g.1414612_1414613insAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGC , CM000667.1:g.1414612_1414613insAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGC	GRCh37
NC_000005.8:g.1467612_1467613insAGGGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGCGGAGAAGGCACTGGGTGGGGGGCCGGGAGGGGCAGGGC	NCBI36
NG_015885.1:g.35937_35938insCCCCTCCCGGCCCCCCACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTGCCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTGCCCTG MANE Select	ENSP00000270349.9:n.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCA...
ENST00000270349.11:c.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTGCCCTG	ENSP00000270349.9:n.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCA...
NM_001044.4:c.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTGCCCTG	NP_001035.1:n.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCT...
NM_001044.5:c.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCTTCTCCGCCCTGCCCCTCCCGGCCCCCCACCCAGTGCCTTCCCTGCCCTG MANE Select	NP_001035.1:n.1156+199_1156+200insCCCCTCCCGGCCCCCCACCCAGTGCCT...