Canonical Allele Identifier: CA112961461
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs146276801

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1410949_1410962del , CM000667.2:g.1410949_1410962del GRCh38
NC_000005.9:g.1411064_1411077del , CM000667.1:g.1411064_1411077del GRCh37
NC_000005.8:g.1464064_1464077del NCBI36
NG_015885.1:g.39470_39483del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1269+284_1269+297del MANE Select ENSP00000270349.9:n.1269+284_1269+297del
ENST00000270349.11:c.1269+284_1269+297del ENSP00000270349.9:n.1269+284_1269+297del
NM_001044.4:c.1269+284_1269+297del NP_001035.1:n.1269+284_1269+297del
NM_001044.5:c.1269+284_1269+297del MANE Select NP_001035.1:n.1269+284_1269+297del