Canonical Allele Identifier: CA867734289

Gene: SLC28A3

Linked Data

• dbSNP Id: rs1356106254
• gnomAD v3: 9-84307005-AAAAAAAAAAAAAAAAGCTTCGTGTGATGGCAC-A
• gnomAD v4: 9-84307005-AAAAAAAAAAAAAAAAGCTTCGTGTGATGGCAC-A
• MyVariant Identifiers: chr9:g.86921921_86921952del (hg19) ; chr9:g.84307006_84307037del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307009_84307040del , CM000671.2:g.84307009_84307040del	GRCh38
NC_000009.11:g.86921924_86921955del , CM000671.1:g.86921924_86921955del	GRCh37
NC_000009.10:g.86111744_86111775del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.243-1692_243-1661del MANE Select	ENSP00000365413.4:n.243-1692_243-1661del
ENST00000376238.4:c.243-1692_243-1661del	ENSP00000365413.4:n.243-1692_243-1661del
ENST00000495823.1:n.445-1692_445-1661del
NM_001199633.1:c.243-1692_243-1661del	NP_001186562.1:n.243-1692_243-1661del
NM_022127.2:c.243-1692_243-1661del	NP_071410.1:n.243-1692_243-1661del
NR_037638.2:n.565-1692_565-1661del
XM_011518905.1:c.418+2592_418+2623del	XP_011517207.1:n.418+2592_418+2623del
XM_011518906.1:c.418+2592_418+2623del	XP_011517208.1:n.418+2592_418+2623del
XM_011518907.1:c.85+2592_85+2623del	XP_011517209.1:n.85+2592_85+2623del
XM_011518909.1:c.418+2592_418+2623del	XP_011517211.1:n.418+2592_418+2623del
XM_011518910.1:c.418+2592_418+2623del	XP_011517212.1:n.418+2592_418+2623del
XR_929832.1:n.545+2592_545+2623del
XM_011518905.2:c.418+2592_418+2623del	XP_011517207.1:n.418+2592_418+2623del
XM_011518906.2:c.418+2592_418+2623del	XP_011517208.1:n.418+2592_418+2623del
XM_011518907.2:c.85+2592_85+2623del	XP_011517209.1:n.85+2592_85+2623del
XM_011518909.2:c.418+2592_418+2623del	XP_011517211.1:n.418+2592_418+2623del
XM_011518910.2:c.418+2592_418+2623del	XP_011517212.1:n.418+2592_418+2623del
XR_929832.2:n.550+2592_550+2623del
NM_001199633.2:c.243-1692_243-1661del MANE Select	NP_001186562.1:n.243-1692_243-1661del
NM_022127.3:c.243-1692_243-1661del	NP_071410.1:n.243-1692_243-1661del
NR_037638.3:n.544-1692_544-1661del