Canonical Allele Identifier: CA1126200675
Gene: SLC28A3 HGNC NCBI

Linked Data

dbSNP Id: rs1825814919

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.84307013_84307014insG , CM000671.2:g.84307013_84307014insG GRCh38
NC_000009.11:g.86921928_86921929insG , CM000671.1:g.86921928_86921929insG GRCh37
NC_000009.10:g.86111748_86111749insG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376238.5:c.243-1669_243-1668insC MANE Select ENSP00000365413.4:n.243-1669_243-1668insC
ENST00000376238.4:c.243-1669_243-1668insC ENSP00000365413.4:n.243-1669_243-1668insC
ENST00000495823.1:n.445-1669_445-1668insC
NM_001199633.1:c.243-1669_243-1668insC NP_001186562.1:n.243-1669_243-1668insC
NM_022127.2:c.243-1669_243-1668insC NP_071410.1:n.243-1669_243-1668insC
NR_037638.2:n.565-1669_565-1668insC
XM_011518905.1:c.418+2615_418+2616insC XP_011517207.1:n.418+2615_418+2616insC
XM_011518906.1:c.418+2615_418+2616insC XP_011517208.1:n.418+2615_418+2616insC
XM_011518907.1:c.85+2615_85+2616insC XP_011517209.1:n.85+2615_85+2616insC
XM_011518909.1:c.418+2615_418+2616insC XP_011517211.1:n.418+2615_418+2616insC
XM_011518910.1:c.418+2615_418+2616insC XP_011517212.1:n.418+2615_418+2616insC
XR_929832.1:n.545+2615_545+2616insC
XM_011518905.2:c.418+2615_418+2616insC XP_011517207.1:n.418+2615_418+2616insC
XM_011518906.2:c.418+2615_418+2616insC XP_011517208.1:n.418+2615_418+2616insC
XM_011518907.2:c.85+2615_85+2616insC XP_011517209.1:n.85+2615_85+2616insC
XM_011518909.2:c.418+2615_418+2616insC XP_011517211.1:n.418+2615_418+2616insC
XM_011518910.2:c.418+2615_418+2616insC XP_011517212.1:n.418+2615_418+2616insC
XR_929832.2:n.550+2615_550+2616insC
NM_001199633.2:c.243-1669_243-1668insC MANE Select NP_001186562.1:n.243-1669_243-1668insC
NM_022127.3:c.243-1669_243-1668insC NP_071410.1:n.243-1669_243-1668insC
NR_037638.3:n.544-1669_544-1668insC