Canonical Allele Identifier: CA588697773

Gene: SLC28A3

Linked Data

• dbSNP Id: rs1363739789
• gnomAD v2: 9-86922046-C-CAAA
• gnomAD v3: 9-84307131-C-CAAA
• gnomAD v4: 9-84307131-C-CAAA
• MyVariant Identifiers: chr9:g.86922046_86922047insAAA (hg19) ; chr9:g.84307131_84307132insAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307131_84307132insAAA , CM000671.2:g.84307131_84307132insAAA	GRCh38
NC_000009.11:g.86922046_86922047insAAA , CM000671.1:g.86922046_86922047insAAA	GRCh37
NC_000009.10:g.86111866_86111867insAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1787_243-1786insTTT MANE Select	ENSP00000365413.4:n.243-1787_243-1786insT...
ENST00000376238.4:c.243-1787_243-1786insTTT	ENSP00000365413.4:n.243-1787_243-1786insT...
ENST00000495823.1:n.445-1787_445-1786insTTT
NM_001199633.1:c.243-1787_243-1786insTTT	NP_001186562.1:n.243-1787_243-1786insTTT
NM_022127.2:c.243-1787_243-1786insTTT	NP_071410.1:n.243-1787_243-1786insTTT
NR_037638.2:n.565-1787_565-1786insTTT
XM_011518905.1:c.418+2497_418+2498insTTT	XP_011517207.1:n.418+2497_418+2498insTTT
XM_011518906.1:c.418+2497_418+2498insTTT	XP_011517208.1:n.418+2497_418+2498insTTT
XM_011518907.1:c.85+2497_85+2498insTTT	XP_011517209.1:n.85+2497_85+2498insTTT
XM_011518909.1:c.418+2497_418+2498insTTT	XP_011517211.1:n.418+2497_418+2498insTTT
XM_011518910.1:c.418+2497_418+2498insTTT	XP_011517212.1:n.418+2497_418+2498insTTT
XR_929832.1:n.545+2497_545+2498insTTT
XM_011518905.2:c.418+2497_418+2498insTTT	XP_011517207.1:n.418+2497_418+2498insTTT
XM_011518906.2:c.418+2497_418+2498insTTT	XP_011517208.1:n.418+2497_418+2498insTTT
XM_011518907.2:c.85+2497_85+2498insTTT	XP_011517209.1:n.85+2497_85+2498insTTT
XM_011518909.2:c.418+2497_418+2498insTTT	XP_011517211.1:n.418+2497_418+2498insTTT
XM_011518910.2:c.418+2497_418+2498insTTT	XP_011517212.1:n.418+2497_418+2498insTTT
XR_929832.2:n.550+2497_550+2498insTTT
NM_001199633.2:c.243-1787_243-1786insTTT MANE Select	NP_001186562.1:n.243-1787_243-1786insTTT
NM_022127.3:c.243-1787_243-1786insTTT	NP_071410.1:n.243-1787_243-1786insTTT
NR_037638.3:n.544-1787_544-1786insTTT