Canonical Allele Identifier: CA625445272
Gene: SLC6A4 HGNC NCBI

Linked Data

dbSNP Id: rs1259183832
gnomAD v2: 17-28551933-AGCTCCTGGAAGAGTAATAC-A
gnomAD v3: 17-30224915-AGCTCCTGGAAGAGTAATAC-A
gnomAD v4: 17-30224915-AGCTCCTGGAAGAGTAATAC-A
MyVariant Identifiers: chr17:g.28551934_28551952del (hg19) chr17:g.30224916_30224934del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30224919_30224937del , CM000679.2:g.30224919_30224937del GRCh38
NC_000017.10:g.28551937_28551955del , CM000679.1:g.28551937_28551955del GRCh37
NC_000017.9:g.25576063_25576081del NCBI36
NG_011747.2:g.16003_16021del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650711.1:c.-220-2019_-220-2001del MANE Select ENSP00000498537.1:n.-220-2019_-220-2001del
ENST00000261707.7:c.-220-2019_-220-2001del ENSP00000261707.3:n.-220-2019_-220-2001del
ENST00000394821.2:c.-220-2019_-220-2001del ENSP00000378298.2:n.-220-2019_-220-2001del
ENST00000401766.6:c.-123-2853_-123-2835del ENSP00000385822.2:n.-123-2853_-123-2835del
NM_001045.5:c.-220-2019_-220-2001del NP_001036.1:n.-220-2019_-220-2001del
NM_001045.6:c.-220-2019_-220-2001del MANE Select NP_001036.1:n.-220-2019_-220-2001del
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