Canonical Allele Identifier: CA1126200917

Gene: SLC28A3

Linked Data

• gnomAD v3: 9-84307132-C-CAAAAAAAA
• gnomAD v4: 9-84307132-C-CAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307141_84307148dup , CM000671.2:g.84307141_84307148dup	GRCh38
NC_000009.11:g.86922056_86922063dup , CM000671.1:g.86922056_86922063dup	GRCh37
NC_000009.10:g.86111876_86111883dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1795_243-1788dup MANE Select	ENSP00000365413.4:n.243-1795_243-1788dup
ENST00000376238.4:c.243-1795_243-1788dup	ENSP00000365413.4:n.243-1795_243-1788dup
ENST00000495823.1:n.445-1795_445-1788dup
NM_001199633.1:c.243-1795_243-1788dup	NP_001186562.1:n.243-1795_243-1788dup
NM_022127.2:c.243-1795_243-1788dup	NP_071410.1:n.243-1795_243-1788dup
NR_037638.2:n.565-1795_565-1788dup
XM_011518905.1:c.418+2489_418+2496dup	XP_011517207.1:n.418+2489_418+2496dup
XM_011518906.1:c.418+2489_418+2496dup	XP_011517208.1:n.418+2489_418+2496dup
XM_011518907.1:c.85+2489_85+2496dup	XP_011517209.1:n.85+2489_85+2496dup
XM_011518909.1:c.418+2489_418+2496dup	XP_011517211.1:n.418+2489_418+2496dup
XM_011518910.1:c.418+2489_418+2496dup	XP_011517212.1:n.418+2489_418+2496dup
XR_929832.1:n.545+2489_545+2496dup
XM_011518905.2:c.418+2489_418+2496dup	XP_011517207.1:n.418+2489_418+2496dup
XM_011518906.2:c.418+2489_418+2496dup	XP_011517208.1:n.418+2489_418+2496dup
XM_011518907.2:c.85+2489_85+2496dup	XP_011517209.1:n.85+2489_85+2496dup
XM_011518909.2:c.418+2489_418+2496dup	XP_011517211.1:n.418+2489_418+2496dup
XM_011518910.2:c.418+2489_418+2496dup	XP_011517212.1:n.418+2489_418+2496dup
XR_929832.2:n.550+2489_550+2496dup
NM_001199633.2:c.243-1795_243-1788dup MANE Select	NP_001186562.1:n.243-1795_243-1788dup
NM_022127.3:c.243-1795_243-1788dup	NP_071410.1:n.243-1795_243-1788dup
NR_037638.3:n.544-1795_544-1788dup