Canonical Allele Identifier: CA1126200644
Gene: SLC28A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.84307020_84307021insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000671.2:g.84307020_84307021insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000009.11:g.86921935_86921936insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000671.1:g.86921935_86921936insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000009.10:g.86111755_86111756insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376238.5:c.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000365413.4:n.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTT...
ENST00000376238.4:c.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000365413.4:n.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTT...
ENST00000495823.1:n.445-1650_445-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001199633.1:c.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001186562.1:n.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTT...
NM_022127.2:c.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_071410.1:n.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NR_037638.2:n.565-1650_565-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_011518905.1:c.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517207.1:n.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011518906.1:c.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517208.1:n.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011518907.1:c.85+2634_85+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517209.1:n.85+2634_85+2635insTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011518909.1:c.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517211.1:n.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011518910.1:c.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517212.1:n.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTT...
XR_929832.1:n.545+2634_545+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_011518905.2:c.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517207.1:n.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011518906.2:c.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517208.1:n.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011518907.2:c.85+2634_85+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517209.1:n.85+2634_85+2635insTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011518909.2:c.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517211.1:n.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011518910.2:c.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011517212.1:n.418+2634_418+2635insTTTTTTTTTTTTTTTTTTTTTTTT...
XR_929832.2:n.550+2634_550+2635insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001199633.2:c.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_001186562.1:n.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTT...
NM_022127.3:c.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_071410.1:n.243-1650_243-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NR_037638.3:n.544-1650_544-1649insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT