Canonical Allele Identifier: CA112970247
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1553989553
MyVariant Identifiers: chr5:g.1443601_1443602insC (hg19) chr5:g.1443486_1443487insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1443487dup , CM000667.2:g.1443487dup GRCh38
NC_000005.9:g.1443602dup , CM000667.1:g.1443602dup GRCh37
NC_000005.8:g.1496602dup NCBI36
NG_015885.1:g.6942dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.-45-245dup MANE Select ENSP00000270349.9:n.-45-245dup
ENST00000270349.11:c.-45-245dup ENSP00000270349.9:n.-45-245dup
NM_001044.4:c.-45-245dup NP_001035.1:n.-45-245dup
NM_001044.5:c.-45-245dup MANE Select NP_001035.1:n.-45-245dup
Search 100 bp 5'
Search 100 bp 3'