Canonical Allele Identifier: CA2612827762

Gene: SLC6A5

Linked Data

• gnomAD v4: 11-20627958-CTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20627961_20627964del , CM000673.2:g.20627961_20627964del	GRCh38
NC_000011.9:g.20649507_20649510del , CM000673.1:g.20649507_20649510del	GRCh37
NC_000011.8:g.20606083_20606086del	NCBI36
NG_013086.1:g.33562_33565del
NG_013086.2:g.33562_33565del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525748.6:c.1396-19_1396-16del MANE Select	ENSP00000434364.2:n.1396-19_1396-16del
ENST00000298923.11:c.*693-19_*693-16del	ENSP00000298923.7:n.*693-19_*693-16del
ENST00000525748.5:c.1396-19_1396-16del	ENSP00000434364.1:n.1396-19_1396-16del
NM_004211.3:c.1396-19_1396-16del	NP_004202.2:n.1396-19_1396-16del
XM_005253225.1:c.694-19_694-16del	XP_005253282.1:n.694-19_694-16del
XM_011520473.1:c.1396-19_1396-16del	XP_011518775.1:n.1396-19_1396-16del
NM_001318369.1:c.694-19_694-16del	NP_001305298.1:n.694-19_694-16del
NM_004211.4:c.1396-19_1396-16del	NP_004202.3:n.1396-19_1396-16del
XM_017018544.2:c.520-19_520-16del	XP_016874033.1:n.520-19_520-16del
XM_017018545.2:c.355-19_355-16del	XP_016874034.1:n.355-19_355-16del
NM_001318369.2:c.694-19_694-16del	NP_001305298.1:n.694-19_694-16del
NM_004211.5:c.1396-19_1396-16del MANE Select	NP_004202.4:n.1396-19_1396-16del