Canonical Allele Identifier: CA2578789676

Gene: SLC22A3

Linked Data

• gnomAD v4: 6-160436898-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436898A>T , CM000668.2:g.160436898A>T	GRCh38
NC_000006.11:g.160857930A>T , CM000668.1:g.160857930A>T	GRCh37
NC_000006.10:g.160777920A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1073+21A>T MANE Select	ENSP00000275300.2:n.1073+21A>T
ENST00000275300.2:c.1073+21A>T	ENSP00000275300.2:n.1073+21A>T
NM_021977.3:c.1073+21A>T	NP_068812.1:n.1073+21A>T
XM_005267106.3:c.680+21A>T	XP_005267163.1:n.680+21A>T
XM_011536075.1:c.617+21A>T	XP_011534377.1:n.617+21A>T
XM_011536076.1:c.617+21A>T	XP_011534378.1:n.617+21A>T
XM_011536077.1:c.617+21A>T	XP_011534379.1:n.617+21A>T
XR_245546.1:n.1018-5863A>T
XM_005267106.5:c.680+21A>T	XP_005267163.1:n.680+21A>T
XM_011536075.2:c.617+21A>T	XP_011534377.1:n.617+21A>T
XM_011536076.3:c.617+21A>T	XP_011534378.1:n.617+21A>T
XM_017011203.2:c.617+21A>T	XP_016866692.1:n.617+21A>T
XR_001743588.1:n.1018-99A>T
XR_001743589.1:n.1018-5863A>T
NM_021977.4:c.1073+21A>T MANE Select	NP_068812.1:n.1073+21A>T