Canonical Allele Identifier: CA465714211

Gene: SLC28A3 SLC28A3-AS1

Linked Data

• dbSNP Id: rs1262329435
• gnomAD v2: 9-86905019-T-C
• gnomAD v3: 9-84290104-T-C
• gnomAD v4: 9-84290104-T-C
• MyVariant Identifiers: chr9:g.86905019T>C (hg19) ; chr9:g.84290104T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84290104T>C , CM000671.2:g.84290104T>C	GRCh38
NC_000009.11:g.86905019T>C , CM000671.1:g.86905019T>C	GRCh37
NC_000009.10:g.86094839T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.1149+50A>G (SLC28A3) MANE Select	ENSP00000365413.4:n.1149+50A>G
ENST00000376238.4:c.1149+50A>G (SLC28A3)	ENSP00000365413.4:n.1149+50A>G
NM_001199633.1:c.1149+50A>G (SLC28A3)	NP_001186562.1:n.1149+50A>G
NM_022127.2:c.1149+50A>G (SLC28A3)	NP_071410.1:n.1149+50A>G
NR_037638.2:n.1471+50A>G (SLC28A3)
XM_011518905.1:c.1233+50A>G (SLC28A3)	XP_011517207.1:n.1233+50A>G
XM_011518906.1:c.1233+50A>G (SLC28A3)	XP_011517208.1:n.1233+50A>G
XM_011518907.1:c.900+50A>G (SLC28A3)	XP_011517209.1:n.900+50A>G
XM_011518908.1:c.510+50A>G (SLC28A3)	XP_011517210.1:n.510+50A>G
XR_929832.1:n.1360+50A>G (SLC28A3)
XR_930032.1:n.636T>C (SLC28A3-AS1)
XR_930033.1:n.520T>C (SLC28A3-AS1)
XM_011518905.2:c.1233+50A>G (SLC28A3)	XP_011517207.1:n.1233+50A>G
XM_011518906.2:c.1233+50A>G (SLC28A3)	XP_011517208.1:n.1233+50A>G
XM_011518907.2:c.900+50A>G (SLC28A3)	XP_011517209.1:n.900+50A>G
XM_011518908.2:c.510+50A>G (SLC28A3)	XP_011517210.1:n.510+50A>G
XR_001746802.1:n.395T>C (SLC28A3-AS1)
XR_001746803.1:n.1147T>C (SLC28A3-AS1)
XR_929832.2:n.1365+50A>G (SLC28A3)
NM_001199633.2:c.1149+50A>G (SLC28A3) MANE Select	NP_001186562.1:n.1149+50A>G
NM_022127.3:c.1149+50A>G (SLC28A3)	NP_071410.1:n.1149+50A>G
NR_037638.3:n.1450+50A>G (SLC28A3)