Canonical Allele Identifier: CA465714235
Gene: SLC28A3 HGNC NCBI
SLC28A3-AS1 HGNC NCBI

Linked Data

gnomAD v4: 9-84290111-G-C
MyVariant Identifiers: chr9:g.86905026G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.84290111G>C , CM000671.2:g.84290111G>C GRCh38
NC_000009.11:g.86905026G>C , CM000671.1:g.86905026G>C GRCh37
NC_000009.10:g.86094846G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376238.5:c.1149+43C>G (SLC28A3) MANE Select ENSP00000365413.4:n.1149+43C>G
ENST00000376238.4:c.1149+43C>G (SLC28A3) ENSP00000365413.4:n.1149+43C>G
NM_001199633.1:c.1149+43C>G (SLC28A3) NP_001186562.1:n.1149+43C>G
NM_022127.2:c.1149+43C>G (SLC28A3) NP_071410.1:n.1149+43C>G
NR_037638.2:n.1471+43C>G (SLC28A3)
XM_011518905.1:c.1233+43C>G (SLC28A3) XP_011517207.1:n.1233+43C>G
XM_011518906.1:c.1233+43C>G (SLC28A3) XP_011517208.1:n.1233+43C>G
XM_011518907.1:c.900+43C>G (SLC28A3) XP_011517209.1:n.900+43C>G
XM_011518908.1:c.510+43C>G (SLC28A3) XP_011517210.1:n.510+43C>G
XR_929832.1:n.1360+43C>G (SLC28A3)
XR_930032.1:n.643G>C (SLC28A3-AS1)
XR_930033.1:n.527G>C (SLC28A3-AS1)
XM_011518905.2:c.1233+43C>G (SLC28A3) XP_011517207.1:n.1233+43C>G
XM_011518906.2:c.1233+43C>G (SLC28A3) XP_011517208.1:n.1233+43C>G
XM_011518907.2:c.900+43C>G (SLC28A3) XP_011517209.1:n.900+43C>G
XM_011518908.2:c.510+43C>G (SLC28A3) XP_011517210.1:n.510+43C>G
XR_001746802.1:n.402G>C (SLC28A3-AS1)
XR_001746803.1:n.1154G>C (SLC28A3-AS1)
XR_929832.2:n.1365+43C>G (SLC28A3)
NM_001199633.2:c.1149+43C>G (SLC28A3) MANE Select NP_001186562.1:n.1149+43C>G
NM_022127.3:c.1149+43C>G (SLC28A3) NP_071410.1:n.1149+43C>G
NR_037638.3:n.1450+43C>G (SLC28A3)