Canonical Allele Identifier: CA727890762

Gene: SLC6A4

Linked Data

• dbSNP Id: rs1196779413
• MyVariant Identifiers: chr17:g.28548494_28548495insT (hg19) ; chr17:g.30221476_30221477insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30221476_30221477insT , CM000679.2:g.30221476_30221477insT	GRCh38
NC_000017.10:g.28548494_28548495insT , CM000679.1:g.28548494_28548495insT	GRCh37
NC_000017.9:g.25572620_25572621insT	NCBI36
NG_011747.2:g.19460_19461insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.343+139_343+140insA MANE Select	ENSP00000498537.1:n.343+139_343+140insA
ENST00000261707.7:c.343+139_343+140insA	ENSP00000261707.3:n.343+139_343+140insA
ENST00000394821.2:c.343+139_343+140insA	ENSP00000378298.2:n.343+139_343+140insA
ENST00000401766.6:c.343+139_343+140insA	ENSP00000385822.2:n.343+139_343+140insA
NM_001045.5:c.343+139_343+140insA	NP_001036.1:n.343+139_343+140insA
NM_001045.6:c.343+139_343+140insA MANE Select	NP_001036.1:n.343+139_343+140insA