Canonical Allele Identifier: CA1677059195

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436901_160436902delinsTA , CM000668.2:g.160436901_160436902delinsTA	GRCh38
NC_000006.11:g.160857933_160857934delinsTA , CM000668.1:g.160857933_160857934delinsTA	GRCh37
NC_000006.10:g.160777923_160777924delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1073+24_1073+25delinsTA MANE Select	ENSP00000275300.2:n.1073+24_1073+25delinsTA
ENST00000275300.2:c.1073+24_1073+25delinsTA	ENSP00000275300.2:n.1073+24_1073+25delinsTA
NM_021977.3:c.1073+24_1073+25delinsTA	NP_068812.1:n.1073+24_1073+25delinsTA
XM_005267106.3:c.680+24_680+25delinsTA	XP_005267163.1:n.680+24_680+25delinsTA
XM_011536075.1:c.617+24_617+25delinsTA	XP_011534377.1:n.617+24_617+25delinsTA
XM_011536076.1:c.617+24_617+25delinsTA	XP_011534378.1:n.617+24_617+25delinsTA
XM_011536077.1:c.617+24_617+25delinsTA	XP_011534379.1:n.617+24_617+25delinsTA
XR_245546.1:n.1018-5860_1018-5859delinsTA
XM_005267106.5:c.680+24_680+25delinsTA	XP_005267163.1:n.680+24_680+25delinsTA
XM_011536075.2:c.617+24_617+25delinsTA	XP_011534377.1:n.617+24_617+25delinsTA
XM_011536076.3:c.617+24_617+25delinsTA	XP_011534378.1:n.617+24_617+25delinsTA
XM_017011203.2:c.617+24_617+25delinsTA	XP_016866692.1:n.617+24_617+25delinsTA
XR_001743588.1:n.1018-96_1018-95delinsTA
XR_001743589.1:n.1018-5860_1018-5859delinsTA
NM_021977.4:c.1073+24_1073+25delinsTA MANE Select	NP_068812.1:n.1073+24_1073+25delinsTA