Canonical Allele Identifier: CA1860477383

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307028G= , CM000671.2:g.84307028G=	GRCh38
NC_000009.11:g.86921943G= , CM000671.1:g.86921943G=	GRCh37
NC_000009.10:g.86111763G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1683C= MANE Select	ENSP00000365413.4:n.243-1683C=
ENST00000376238.4:c.243-1683C=	ENSP00000365413.4:n.243-1683C=
ENST00000495823.1:n.445-1683C=
NM_001199633.1:c.243-1683C=	NP_001186562.1:n.243-1683C=
NM_022127.2:c.243-1683C=	NP_071410.1:n.243-1683C=
NR_037638.2:n.565-1683C=
XM_011518905.1:c.418+2601C=	XP_011517207.1:n.418+2601C=
XM_011518906.1:c.418+2601C=	XP_011517208.1:n.418+2601C=
XM_011518907.1:c.85+2601C=	XP_011517209.1:n.85+2601C=
XM_011518909.1:c.418+2601C=	XP_011517211.1:n.418+2601C=
XM_011518910.1:c.418+2601C=	XP_011517212.1:n.418+2601C=
XR_929832.1:n.545+2601C=
XM_011518905.2:c.418+2601C=	XP_011517207.1:n.418+2601C=
XM_011518906.2:c.418+2601C=	XP_011517208.1:n.418+2601C=
XM_011518907.2:c.85+2601C=	XP_011517209.1:n.85+2601C=
XM_011518909.2:c.418+2601C=	XP_011517211.1:n.418+2601C=
XM_011518910.2:c.418+2601C=	XP_011517212.1:n.418+2601C=
XR_929832.2:n.550+2601C=
NM_001199633.2:c.243-1683C= MANE Select	NP_001186562.1:n.243-1683C=
NM_022127.3:c.243-1683C=	NP_071410.1:n.243-1683C=
NR_037638.3:n.544-1683C=