Canonical Allele Identifier: CA1860470508

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84290204C= , CM000671.2:g.84290204C=	GRCh38
NC_000009.11:g.86905119C= , CM000671.1:g.86905119C=	GRCh37
NC_000009.10:g.86094939C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001199633.2:c.1099G= MANE Select	NP_001186562.1:p.Gly367=
ENST00000376238.5:c.1099G= MANE Select	ENSP00000365413.4:p.Gly367=
NM_001199633.1:c.1099G=	NP_001186562.1:p.Gly367=
NM_022127.2:c.1099G=	NP_071410.1:p.Gly367=
NM_022127.3:c.1099G=	NP_071410.1:p.Gly367=
NR_037638.2:n.1421G=
NR_037638.3:n.1400G=
ENST00000376238.4:c.1099G=	ENSP00000365413.4:p.Gly367=
XM_011518905.1:c.1183G=	XP_011517207.1:p.Gly395=
XM_011518905.2:c.1183G=	XP_011517207.1:p.Gly395=
XM_011518906.1:c.1183G=	XP_011517208.1:p.Gly395=
XM_011518906.2:c.1183G=	XP_011517208.1:p.Gly395=
XM_011518907.1:c.850G=	XP_011517209.1:p.Gly284=
XM_011518907.2:c.850G=	XP_011517209.1:p.Gly284=
XM_011518908.1:c.460G=	XP_011517210.1:p.Gly154=
XM_011518908.2:c.460G=	XP_011517210.1:p.Gly154=
XM_011518910.1:c.*116G=	XP_011517212.1:n.*116G=
XM_011518910.2:c.*116G=	XP_011517212.1:n.*116G=
XR_929832.1:n.1310G=
XR_929832.2:n.1315G=