Canonical Allele Identifier: CA1956619712

Gene: SLC6A5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20627970_20627971delinsTG , CM000673.2:g.20627970_20627971delinsTG	GRCh38
NC_000011.9:g.20649516_20649517delinsTG , CM000673.1:g.20649516_20649517delinsTG	GRCh37
NC_000011.8:g.20606092_20606093delinsTG	NCBI36
NG_013086.1:g.33571_33572delinsTG
NG_013086.2:g.33571_33572delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000525748.6:c.1396-10_1396-9delinsTG MANE Select	ENSP00000434364.2:n.1396-10_1396-9delinsTG
ENST00000298923.11:c.*693-10_*693-9delinsTG	ENSP00000298923.7:n.*693-10_*693-9delinsTG
ENST00000525748.5:c.1396-10_1396-9delinsTG	ENSP00000434364.1:n.1396-10_1396-9delinsTG
NM_004211.3:c.1396-10_1396-9delinsTG	NP_004202.2:n.1396-10_1396-9delinsTG
XM_005253225.1:c.694-10_694-9delinsTG	XP_005253282.1:n.694-10_694-9delinsTG
XM_011520473.1:c.1396-10_1396-9delinsTG	XP_011518775.1:n.1396-10_1396-9delinsTG
NM_001318369.1:c.694-10_694-9delinsTG	NP_001305298.1:n.694-10_694-9delinsTG
NM_004211.4:c.1396-10_1396-9delinsTG	NP_004202.3:n.1396-10_1396-9delinsTG
XM_017018544.2:c.520-10_520-9delinsTG	XP_016874033.1:n.520-10_520-9delinsTG
XM_017018545.2:c.355-10_355-9delinsTG	XP_016874034.1:n.355-10_355-9delinsTG
NM_001318369.2:c.694-10_694-9delinsTG	NP_001305298.1:n.694-10_694-9delinsTG
NM_004211.5:c.1396-10_1396-9delinsTG MANE Select	NP_004202.4:n.1396-10_1396-9delinsTG