Canonical Allele Identifier: CA195482151

Gene: SLC28A3

Linked Data

• dbSNP Id: rs1040514295
• MyVariant Identifiers: chr9:g.84307153A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84307153A>T , CM000671.2:g.84307153A>T	GRCh38
NC_000009.11:g.86922068A>T , CM000671.1:g.86922068A>T	GRCh37
NC_000009.10:g.86111888A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.243-1808T>A MANE Select	ENSP00000365413.4:n.243-1808T>A
ENST00000376238.4:c.243-1808T>A	ENSP00000365413.4:n.243-1808T>A
ENST00000495823.1:n.445-1808T>A
NM_001199633.1:c.243-1808T>A	NP_001186562.1:n.243-1808T>A
NM_022127.2:c.243-1808T>A	NP_071410.1:n.243-1808T>A
NR_037638.2:n.565-1808T>A
XM_011518905.1:c.418+2476T>A	XP_011517207.1:n.418+2476T>A
XM_011518906.1:c.418+2476T>A	XP_011517208.1:n.418+2476T>A
XM_011518907.1:c.85+2476T>A	XP_011517209.1:n.85+2476T>A
XM_011518909.1:c.418+2476T>A	XP_011517211.1:n.418+2476T>A
XM_011518910.1:c.418+2476T>A	XP_011517212.1:n.418+2476T>A
XR_929832.1:n.545+2476T>A
XM_011518905.2:c.418+2476T>A	XP_011517207.1:n.418+2476T>A
XM_011518906.2:c.418+2476T>A	XP_011517208.1:n.418+2476T>A
XM_011518907.2:c.85+2476T>A	XP_011517209.1:n.85+2476T>A
XM_011518909.2:c.418+2476T>A	XP_011517211.1:n.418+2476T>A
XM_011518910.2:c.418+2476T>A	XP_011517212.1:n.418+2476T>A
XR_929832.2:n.550+2476T>A
NM_001199633.2:c.243-1808T>A MANE Select	NP_001186562.1:n.243-1808T>A
NM_022127.3:c.243-1808T>A	NP_071410.1:n.243-1808T>A
NR_037638.3:n.544-1808T>A