Canonical Allele Identifier: CA674473384

Gene: SLC6A5

Linked Data

• dbSNP Id: rs1270619107
• gnomAD v3: 11-20638330-AG-A
• gnomAD v4: 11-20638330-AG-A
• MyVariant Identifiers: chr11:g.20659877del (hg19) ; chr11:g.20638331del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20638334del , CM000673.2:g.20638334del	GRCh38
NC_000011.9:g.20659880del , CM000673.1:g.20659880del	GRCh37
NC_000011.8:g.20616456del	NCBI36
NG_013086.1:g.43935del
NG_013086.2:g.43935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1870-125del MANE Select	ENSP00000434364.2:n.1870-125del
ENST00000298923.11:c.*1167-125del	ENSP00000298923.7:n.*1167-125del
ENST00000525748.5:c.1870-125del	ENSP00000434364.1:n.1870-125del
ENST00000528440.1:n.401-125del
NM_004211.3:c.1870-125del	NP_004202.2:n.1870-125del
XM_005253225.1:c.1168-125del	XP_005253282.1:n.1168-125del
XM_011520473.1:c.1870-125del	XP_011518775.1:n.1870-125del
NM_001318369.1:c.1168-125del	NP_001305298.1:n.1168-125del
NM_004211.4:c.1870-125del	NP_004202.3:n.1870-125del
XM_017018544.2:c.994-125del	XP_016874033.1:n.994-125del
XM_017018545.2:c.829-125del	XP_016874034.1:n.829-125del
NM_001318369.2:c.1168-125del	NP_001305298.1:n.1168-125del
NM_004211.5:c.1870-125del MANE Select	NP_004202.4:n.1870-125del