Canonical Allele Identifier: CA1677059275

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437065_160437066delinsTA , CM000668.2:g.160437065_160437066delinsTA	GRCh38
NC_000006.11:g.160858097_160858098delinsTA , CM000668.1:g.160858097_160858098delinsTA	GRCh37
NC_000006.10:g.160778087_160778088delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1142_1143delinsTA MANE Select	ENSP00000275300.2:p.Ile381=
ENST00000275300.2:c.1142_1143delinsTA	ENSP00000275300.2:p.Ile381=
NM_021977.3:c.1142_1143delinsTA	NP_068812.1:p.Ile381=
XM_005267106.3:c.749_750delinsTA	XP_005267163.1:p.Ile250=
XM_011536075.1:c.686_687delinsTA	XP_011534377.1:p.Ile229=
XM_011536076.1:c.686_687delinsTA	XP_011534378.1:p.Ile229=
XM_011536077.1:c.686_687delinsTA	XP_011534379.1:p.Ile229=
XR_245546.1:n.1018-5696_1018-5695delinsTA
XM_005267106.5:c.749_750delinsTA	XP_005267163.1:p.Ile250=
XM_011536075.2:c.686_687delinsTA	XP_011534377.1:p.Ile229=
XM_011536076.3:c.686_687delinsTA	XP_011534378.1:p.Ile229=
XM_017011203.2:c.686_687delinsTA	XP_016866692.1:p.Ile229=
XR_001743588.1:n.1086_1087delinsTA
XR_001743589.1:n.1018-5696_1018-5695delinsTA
NM_021977.4:c.1142_1143delinsTA MANE Select	NP_068812.1:p.Ile381=