Canonical Allele Identifier: CA1126200849

Gene: SLC28A3

Linked Data

• gnomAD v3: 9-84307130-ACC-A
• gnomAD v4: 9-84307130-ACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307131_84307132del , CM000671.2:g.84307131_84307132del	GRCh38
NC_000009.11:g.86922046_86922047del , CM000671.1:g.86922046_86922047del	GRCh37
NC_000009.10:g.86111866_86111867del	NCBI36

Transcript Alleles

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