Canonical Allele Identifier: CA1860477341

Gene: SLC28A3

Linked Data

• dbSNP Id: rs1825814285

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307004_84307005insG , CM000671.2:g.84307004_84307005insG	GRCh38
NC_000009.11:g.86921919_86921920insG , CM000671.1:g.86921919_86921920insG	GRCh37
NC_000009.10:g.86111739_86111740insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.243-1660_243-1659insC MANE Select	ENSP00000365413.4:n.243-1660_243-1659insC
ENST00000376238.4:c.243-1660_243-1659insC	ENSP00000365413.4:n.243-1660_243-1659insC
ENST00000495823.1:n.445-1660_445-1659insC
NM_001199633.1:c.243-1660_243-1659insC	NP_001186562.1:n.243-1660_243-1659insC
NM_022127.2:c.243-1660_243-1659insC	NP_071410.1:n.243-1660_243-1659insC
NR_037638.2:n.565-1660_565-1659insC
XM_011518905.1:c.418+2624_418+2625insC	XP_011517207.1:n.418+2624_418+2625insC
XM_011518906.1:c.418+2624_418+2625insC	XP_011517208.1:n.418+2624_418+2625insC
XM_011518907.1:c.85+2624_85+2625insC	XP_011517209.1:n.85+2624_85+2625insC
XM_011518909.1:c.418+2624_418+2625insC	XP_011517211.1:n.418+2624_418+2625insC
XM_011518910.1:c.418+2624_418+2625insC	XP_011517212.1:n.418+2624_418+2625insC
XR_929832.1:n.545+2624_545+2625insC
XM_011518905.2:c.418+2624_418+2625insC	XP_011517207.1:n.418+2624_418+2625insC
XM_011518906.2:c.418+2624_418+2625insC	XP_011517208.1:n.418+2624_418+2625insC
XM_011518907.2:c.85+2624_85+2625insC	XP_011517209.1:n.85+2624_85+2625insC
XM_011518909.2:c.418+2624_418+2625insC	XP_011517211.1:n.418+2624_418+2625insC
XM_011518910.2:c.418+2624_418+2625insC	XP_011517212.1:n.418+2624_418+2625insC
XR_929832.2:n.550+2624_550+2625insC
NM_001199633.2:c.243-1660_243-1659insC MANE Select	NP_001186562.1:n.243-1660_243-1659insC
NM_022127.3:c.243-1660_243-1659insC	NP_071410.1:n.243-1660_243-1659insC
NR_037638.3:n.544-1660_544-1659insC