Canonical Allele Identifier: CA2539018964

Gene: SLC28A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84306925_84306926insGGCG , CM000671.2:g.84306925_84306926insGGCG	GRCh38
NC_000009.11:g.86921840_86921841insGGCG , CM000671.1:g.86921840_86921841insGGCG	GRCh37
NC_000009.10:g.86111660_86111661insGGCG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1581_243-1580insCGCC MANE Select	ENSP00000365413.4:n.243-1581_243-1580insCGCC
ENST00000376238.4:c.243-1581_243-1580insCGCC	ENSP00000365413.4:n.243-1581_243-1580insCGCC
ENST00000495823.1:n.445-1581_445-1580insCGCC
NM_001199633.1:c.243-1581_243-1580insCGCC	NP_001186562.1:n.243-1581_243-1580insCGCC
NM_022127.2:c.243-1581_243-1580insCGCC	NP_071410.1:n.243-1581_243-1580insCGCC
NR_037638.2:n.565-1581_565-1580insCGCC
XM_011518905.1:c.418+2703_418+2704insCGCC	XP_011517207.1:n.418+2703_418+2704insCGCC
XM_011518906.1:c.418+2703_418+2704insCGCC	XP_011517208.1:n.418+2703_418+2704insCGCC
XM_011518907.1:c.85+2703_85+2704insCGCC	XP_011517209.1:n.85+2703_85+2704insCGCC
XM_011518909.1:c.418+2703_418+2704insCGCC	XP_011517211.1:n.418+2703_418+2704insCGCC
XM_011518910.1:c.418+2703_418+2704insCGCC	XP_011517212.1:n.418+2703_418+2704insCGCC
XR_929832.1:n.545+2703_545+2704insCGCC
XM_011518905.2:c.418+2703_418+2704insCGCC	XP_011517207.1:n.418+2703_418+2704insCGCC
XM_011518906.2:c.418+2703_418+2704insCGCC	XP_011517208.1:n.418+2703_418+2704insCGCC
XM_011518907.2:c.85+2703_85+2704insCGCC	XP_011517209.1:n.85+2703_85+2704insCGCC
XM_011518909.2:c.418+2703_418+2704insCGCC	XP_011517211.1:n.418+2703_418+2704insCGCC
XM_011518910.2:c.418+2703_418+2704insCGCC	XP_011517212.1:n.418+2703_418+2704insCGCC
XR_929832.2:n.550+2703_550+2704insCGCC
NM_001199633.2:c.243-1581_243-1580insCGCC MANE Select	NP_001186562.1:n.243-1581_243-1580insCGCC
NM_022127.3:c.243-1581_243-1580insCGCC	NP_071410.1:n.243-1581_243-1580insCGCC
NR_037638.3:n.544-1581_544-1580insCGCC