Canonical Allele Identifier: CA195499183

Gene: SLC28A3

Linked Data

• dbSNP Id: rs34133557
• MyVariant Identifiers: chr9:g.86944519_86944520insG (hg19) ; chr9:g.84329604_84329605insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84329607dup , CM000671.2:g.84329607dup	GRCh38
NC_000009.11:g.86944522dup , CM000671.1:g.86944522dup	GRCh37
NC_000009.10:g.86134342dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376238.5:c.60+10969dup MANE Select	ENSP00000365413.4:n.60+10969dup
ENST00000376238.4:c.60+10969dup	ENSP00000365413.4:n.60+10969dup
ENST00000495823.1:n.86+10969dup
NM_001199633.1:c.60+10969dup	NP_001186562.1:n.60+10969dup
NM_022127.2:c.60+10969dup	NP_071410.1:n.60+10969dup
NR_037638.2:n.206+10969dup
XM_011518905.1:c.60+10969dup	XP_011517207.1:n.60+10969dup
XM_011518906.1:c.60+10969dup	XP_011517208.1:n.60+10969dup
XM_011518907.1:c.-97-16151dup	XP_011517209.1:n.-97-16151dup
XM_011518909.1:c.60+10969dup	XP_011517211.1:n.60+10969dup
XM_011518910.1:c.60+10969dup	XP_011517212.1:n.60+10969dup
XR_929832.1:n.187+10969dup
XM_011518905.2:c.60+10969dup	XP_011517207.1:n.60+10969dup
XM_011518906.2:c.60+10969dup	XP_011517208.1:n.60+10969dup
XM_011518907.2:c.-97-16151dup	XP_011517209.1:n.-97-16151dup
XM_011518909.2:c.60+10969dup	XP_011517211.1:n.60+10969dup
XM_011518910.2:c.60+10969dup	XP_011517212.1:n.60+10969dup
XR_929832.2:n.192+10969dup
NM_001199633.2:c.60+10969dup MANE Select	NP_001186562.1:n.60+10969dup
NM_022127.3:c.60+10969dup	NP_071410.1:n.60+10969dup
NR_037638.3:n.185+10969dup