Canonical Allele Identifier: CA289284522

Gene: SLC6A4

Linked Data

• dbSNP Id: rs369502939
• MyVariant Identifiers: chr17:g.28551918_28551919del (hg19) ; chr17:g.30224900_30224901del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30224900_30224901del , CM000679.2:g.30224900_30224901del	GRCh38
NC_000017.10:g.28551918_28551919del , CM000679.1:g.28551918_28551919del	GRCh37
NC_000017.9:g.25576044_25576045del	NCBI36
NG_011747.2:g.16036_16037del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650711.1:c.-220-1986_-220-1985del MANE Select	ENSP00000498537.1:n.-220-1986_-220-1985del
ENST00000261707.7:c.-220-1986_-220-1985del	ENSP00000261707.3:n.-220-1986_-220-1985del
ENST00000394821.2:c.-220-1986_-220-1985del	ENSP00000378298.2:n.-220-1986_-220-1985del
ENST00000401766.6:c.-123-2820_-123-2819del	ENSP00000385822.2:n.-123-2820_-123-2819del
NM_001045.5:c.-220-1986_-220-1985del	NP_001036.1:n.-220-1986_-220-1985del
NM_001045.6:c.-220-1986_-220-1985del MANE Select	NP_001036.1:n.-220-1986_-220-1985del