Canonical Allele Identifier: CA1860472445

Gene: SLC28A3

Linked Data

• dbSNP Id: rs1588576394

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84294712T>C , CM000671.2:g.84294712T>C	GRCh38
NC_000009.11:g.86909627T>C , CM000671.1:g.86909627T>C	GRCh37
NC_000009.10:g.86099447T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.862-437A>G MANE Select	ENSP00000365413.4:n.862-437A>G
ENST00000376238.4:c.862-437A>G	ENSP00000365413.4:n.862-437A>G
NM_001199633.1:c.862-437A>G	NP_001186562.1:n.862-437A>G
NM_022127.2:c.862-437A>G	NP_071410.1:n.862-437A>G
NR_037638.2:n.1184-437A>G
XM_011518905.1:c.946-437A>G	XP_011517207.1:n.946-437A>G
XM_011518906.1:c.946-437A>G	XP_011517208.1:n.946-437A>G
XM_011518907.1:c.613-437A>G	XP_011517209.1:n.613-437A>G
XM_011518908.1:c.223-437A>G	XP_011517210.1:n.223-437A>G
XM_011518909.1:c.946-437A>G	XP_011517211.1:n.946-437A>G
XM_011518910.1:c.946-437A>G	XP_011517212.1:n.946-437A>G
XR_929832.1:n.1073-437A>G
XM_011518905.2:c.946-437A>G	XP_011517207.1:n.946-437A>G
XM_011518906.2:c.946-437A>G	XP_011517208.1:n.946-437A>G
XM_011518907.2:c.613-437A>G	XP_011517209.1:n.613-437A>G
XM_011518908.2:c.223-437A>G	XP_011517210.1:n.223-437A>G
XM_011518909.2:c.946-437A>G	XP_011517211.1:n.946-437A>G
XM_011518910.2:c.946-437A>G	XP_011517212.1:n.946-437A>G
XR_929832.2:n.1078-437A>G
NM_001199633.2:c.862-437A>G MANE Select	NP_001186562.1:n.862-437A>G
NM_022127.3:c.862-437A>G	NP_071410.1:n.862-437A>G
NR_037638.3:n.1163-437A>G