Canonical Allele Identifier: CA2719865255

Gene: SLC28A3

Linked Data

• dbSNP Id: rs2118211308

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84294574C>G , CM000671.2:g.84294574C>G	GRCh38
NC_000009.11:g.86909489C>G , CM000671.1:g.86909489C>G	GRCh37
NC_000009.10:g.86099309C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.862-299G>C MANE Select	ENSP00000365413.4:n.862-299G>C
ENST00000376238.4:c.862-299G>C	ENSP00000365413.4:n.862-299G>C
NM_001199633.1:c.862-299G>C	NP_001186562.1:n.862-299G>C
NM_022127.2:c.862-299G>C	NP_071410.1:n.862-299G>C
NR_037638.2:n.1184-299G>C
XM_011518905.1:c.946-299G>C	XP_011517207.1:n.946-299G>C
XM_011518906.1:c.946-299G>C	XP_011517208.1:n.946-299G>C
XM_011518907.1:c.613-299G>C	XP_011517209.1:n.613-299G>C
XM_011518908.1:c.223-299G>C	XP_011517210.1:n.223-299G>C
XM_011518909.1:c.946-299G>C	XP_011517211.1:n.946-299G>C
XM_011518910.1:c.946-299G>C	XP_011517212.1:n.946-299G>C
XR_929832.1:n.1073-299G>C
XM_011518905.2:c.946-299G>C	XP_011517207.1:n.946-299G>C
XM_011518906.2:c.946-299G>C	XP_011517208.1:n.946-299G>C
XM_011518907.2:c.613-299G>C	XP_011517209.1:n.613-299G>C
XM_011518908.2:c.223-299G>C	XP_011517210.1:n.223-299G>C
XM_011518909.2:c.946-299G>C	XP_011517211.1:n.946-299G>C
XM_011518910.2:c.946-299G>C	XP_011517212.1:n.946-299G>C
XR_929832.2:n.1078-299G>C
NM_001199633.2:c.862-299G>C MANE Select	NP_001186562.1:n.862-299G>C
NM_022127.3:c.862-299G>C	NP_071410.1:n.862-299G>C
NR_037638.3:n.1163-299G>C