Canonical Allele Identifier: CA1522626585

Gene: SLC6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1414386_1414425delinsAAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGGAG , CM000667.2:g.1414386_1414425delinsAAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGGAG	GRCh38
NC_000005.9:g.1414501_1414540delinsAAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGGAG , CM000667.1:g.1414501_1414540delinsAAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGGAG	GRCh37
NC_000005.8:g.1467501_1467540delinsAAAGGCACTGGGTGGGGGGGCCTGGAGGGGCAGGGCGGAG	NCBI36
NG_015885.1:g.36004_36043delinsCTCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.1156+266_1156+305delinsCTCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTTT MANE Select	ENSP00000270349.9:n.1156+266_1156+305delinsCTCCGCCCTGCCCCTCCA...
ENST00000270349.11:c.1156+266_1156+305delinsCTCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTTT	ENSP00000270349.9:n.1156+266_1156+305delinsCTCCGCCCTGCCCCTCCA...
NM_001044.4:c.1156+266_1156+305delinsCTCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTTT	NP_001035.1:n.1156+266_1156+305delinsCTCCGCCCTGCCCCTCCAGGCCCC...
NM_001044.5:c.1156+266_1156+305delinsCTCCGCCCTGCCCCTCCAGGCCCCCCCACCCAGTGCCTTT MANE Select	NP_001035.1:n.1156+266_1156+305delinsCTCCGCCCTGCCCCTCCAGGCCCC...