Canonical Allele Identifier: CA1522626634
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414399_1414437delinsGGGGGGGCCTGGAGGGGCAGGGCGGAGAAGGCACTGGGT , CM000667.2:g.1414399_1414437delinsGGGGGGGCCTGGAGGGGCAGGGCGGAGAAGGCACTGGGT GRCh38
NC_000005.9:g.1414514_1414552delinsGGGGGGGCCTGGAGGGGCAGGGCGGAGAAGGCACTGGGT , CM000667.1:g.1414514_1414552delinsGGGGGGGCCTGGAGGGGCAGGGCGGAGAAGGCACTGGGT GRCh37
NC_000005.8:g.1467514_1467552delinsGGGGGGGCCTGGAGGGGCAGGGCGGAGAAGGCACTGGGT NCBI36
NG_015885.1:g.35992_36030delinsACCCAGTGCCTTCTCCGCCCTGCCCCTCCAGGCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+254_1156+292delinsACCCAGTGCCTTCTCCGCCCTGCCCCTCCAGGCCCCCCC MANE Select ENSP00000270349.9:n.1156+254_1156+292delinsACCCAGTGCCTTCTCCGC...
ENST00000270349.11:c.1156+254_1156+292delinsACCCAGTGCCTTCTCCGCCCTGCCCCTCCAGGCCCCCCC ENSP00000270349.9:n.1156+254_1156+292delinsACCCAGTGCCTTCTCCGC...
NM_001044.4:c.1156+254_1156+292delinsACCCAGTGCCTTCTCCGCCCTGCCCCTCCAGGCCCCCCC NP_001035.1:n.1156+254_1156+292delinsACCCAGTGCCTTCTCCGCCCTGCC...
NM_001044.5:c.1156+254_1156+292delinsACCCAGTGCCTTCTCCGCCCTGCCCCTCCAGGCCCCCCC MANE Select NP_001035.1:n.1156+254_1156+292delinsACCCAGTGCCTTCTCCGCCCTGCC...