Canonical Allele Identifier: CA195482076
Gene: SLC28A3 HGNC NCBI

Linked Data

dbSNP Id: rs1009407497

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.84307052dup , CM000671.2:g.84307052dup GRCh38
NC_000009.11:g.86921967dup , CM000671.1:g.86921967dup GRCh37
NC_000009.10:g.86111787dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376238.5:c.243-1707dup MANE Select ENSP00000365413.4:n.243-1707dup
ENST00000376238.4:c.243-1707dup ENSP00000365413.4:n.243-1707dup
ENST00000495823.1:n.445-1707dup
NM_001199633.1:c.243-1707dup NP_001186562.1:n.243-1707dup
NM_022127.2:c.243-1707dup NP_071410.1:n.243-1707dup
NR_037638.2:n.565-1707dup
XM_011518905.1:c.418+2577dup XP_011517207.1:n.418+2577dup
XM_011518906.1:c.418+2577dup XP_011517208.1:n.418+2577dup
XM_011518907.1:c.85+2577dup XP_011517209.1:n.85+2577dup
XM_011518909.1:c.418+2577dup XP_011517211.1:n.418+2577dup
XM_011518910.1:c.418+2577dup XP_011517212.1:n.418+2577dup
XR_929832.1:n.545+2577dup
XM_011518905.2:c.418+2577dup XP_011517207.1:n.418+2577dup
XM_011518906.2:c.418+2577dup XP_011517208.1:n.418+2577dup
XM_011518907.2:c.85+2577dup XP_011517209.1:n.85+2577dup
XM_011518909.2:c.418+2577dup XP_011517211.1:n.418+2577dup
XM_011518910.2:c.418+2577dup XP_011517212.1:n.418+2577dup
XR_929832.2:n.550+2577dup
NM_001199633.2:c.243-1707dup MANE Select NP_001186562.1:n.243-1707dup
NM_022127.3:c.243-1707dup NP_071410.1:n.243-1707dup
NR_037638.3:n.544-1707dup