Canonical Allele Identifier: CA1860477354
Gene: SLC28A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.84307019_84307021delinsAAG , CM000671.2:g.84307019_84307021delinsAAG GRCh38
NC_000009.11:g.86921934_86921936delinsAAG , CM000671.1:g.86921934_86921936delinsAAG GRCh37
NC_000009.10:g.86111754_86111756delinsAAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376238.5:c.243-1676_243-1674delinsCTT MANE Select ENSP00000365413.4:n.243-1676_243-1674deli...
ENST00000376238.4:c.243-1676_243-1674delinsCTT ENSP00000365413.4:n.243-1676_243-1674deli...
ENST00000495823.1:n.445-1676_445-1674delinsCTT
NM_001199633.1:c.243-1676_243-1674delinsCTT NP_001186562.1:n.243-1676_243-1674delinsC...
NM_022127.2:c.243-1676_243-1674delinsCTT NP_071410.1:n.243-1676_243-1674delinsCTT
NR_037638.2:n.565-1676_565-1674delinsCTT
XM_011518905.1:c.418+2608_418+2610delinsCTT XP_011517207.1:n.418+2608_418+2610delinsC...
XM_011518906.1:c.418+2608_418+2610delinsCTT XP_011517208.1:n.418+2608_418+2610delinsC...
XM_011518907.1:c.85+2608_85+2610delinsCTT XP_011517209.1:n.85+2608_85+2610delinsCTT...
XM_011518909.1:c.418+2608_418+2610delinsCTT XP_011517211.1:n.418+2608_418+2610delinsC...
XM_011518910.1:c.418+2608_418+2610delinsCTT XP_011517212.1:n.418+2608_418+2610delinsC...
XR_929832.1:n.545+2608_545+2610delinsCTT
XM_011518905.2:c.418+2608_418+2610delinsCTT XP_011517207.1:n.418+2608_418+2610delinsC...
XM_011518906.2:c.418+2608_418+2610delinsCTT XP_011517208.1:n.418+2608_418+2610delinsC...
XM_011518907.2:c.85+2608_85+2610delinsCTT XP_011517209.1:n.85+2608_85+2610delinsCTT...
XM_011518909.2:c.418+2608_418+2610delinsCTT XP_011517211.1:n.418+2608_418+2610delinsC...
XM_011518910.2:c.418+2608_418+2610delinsCTT XP_011517212.1:n.418+2608_418+2610delinsC...
XR_929832.2:n.550+2608_550+2610delinsCTT
NM_001199633.2:c.243-1676_243-1674delinsCTT MANE Select NP_001186562.1:n.243-1676_243-1674delinsC...
NM_022127.3:c.243-1676_243-1674delinsCTT NP_071410.1:n.243-1676_243-1674delinsCTT
NR_037638.3:n.544-1676_544-1674delinsCTT