Canonical Allele Identifier: CA557565987
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1208833182
gnomAD v2: 5-1414506-CACT-C
gnomAD v3: 5-1414391-CACT-C
gnomAD v4: 5-1414391-CACT-C
MyVariant Identifiers: chr5:g.1414507_1414509del (hg19) chr5:g.1414392_1414394del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414392_1414394del , CM000667.2:g.1414392_1414394del GRCh38
NC_000005.9:g.1414507_1414509del , CM000667.1:g.1414507_1414509del GRCh37
NC_000005.8:g.1467507_1467509del NCBI36
NG_015885.1:g.36035_36037del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+297_1156+299del MANE Select ENSP00000270349.9:n.1156+297_1156+299del
ENST00000270349.11:c.1156+297_1156+299del ENSP00000270349.9:n.1156+297_1156+299del
NM_001044.4:c.1156+297_1156+299del NP_001035.1:n.1156+297_1156+299del
NM_001044.5:c.1156+297_1156+299del MANE Select NP_001035.1:n.1156+297_1156+299del
Search 100 bp 5'
Search 100 bp 3'