Canonical Allele Identifier: CA727889911

Gene: SLC6A4

Linked Data

• dbSNP Id: rs1222712417
• MyVariant Identifiers: chr17:g.28546790_28546791del (hg19) ; chr17:g.30219772_30219773del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30219772_30219773del , CM000679.2:g.30219772_30219773del	GRCh38
NC_000017.10:g.28546790_28546791del , CM000679.1:g.28546790_28546791del	GRCh37
NC_000017.9:g.25570916_25570917del	NCBI36
NG_011747.2:g.21164_21165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.344-842_344-841del MANE Select	ENSP00000498537.1:n.344-842_344-841del
ENST00000261707.7:c.344-842_344-841del	ENSP00000261707.3:n.344-842_344-841del
ENST00000394821.2:c.344-842_344-841del	ENSP00000378298.2:n.344-842_344-841del
ENST00000401766.6:c.344-842_344-841del	ENSP00000385822.2:n.344-842_344-841del
NM_001045.5:c.344-842_344-841del	NP_001036.1:n.344-842_344-841del
NM_001045.6:c.344-842_344-841del MANE Select	NP_001036.1:n.344-842_344-841del