Canonical Allele Identifier: CA393375983

Gene: SLC28A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84935465C>G , CM000677.2:g.84935465C>G	GRCh38
NC_000015.9:g.85478696C>G , CM000677.1:g.85478696C>G	GRCh37
NC_000015.8:g.83279700C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004213.5:c.1528C>G MANE Select	NP_004204.3:p.Arg510Gly
ENST00000394573.6:c.1528C>G MANE Select	ENSP00000378074.1:p.Arg510Gly
NM_001287761.1:c.1084-7980C>G	NP_001274690.1:n.1084-7980C>G
NM_001287761.2:c.1084-7980C>G	NP_001274690.1:n.1084-7980C>G
NM_001287762.1:c.1528C>G	NP_001274691.1:p.Arg510Gly
NM_001287762.2:c.1528C>G	NP_001274691.1:p.Arg510Gly
NM_001321721.1:c.1528C>G	NP_001308650.1:p.Arg510Gly
NM_001321721.2:c.1528C>G	NP_001308650.1:p.Arg510Gly
NM_001321722.1:c.1528C>G	NP_001308651.1:p.Arg510Gly
NM_001321722.2:c.1528C>G	NP_001308651.1:p.Arg510Gly
NM_004213.4:c.1528C>G	NP_004204.3:p.Arg510Gly
ENST00000286749.3:c.1528C>G	ENSP00000286749.3:p.Arg510Gly
ENST00000394573.5:c.1528C>G	ENSP00000378074.1:p.Arg510Gly
ENST00000538177.5:c.1084-7980C>G	ENSP00000443752.1:n.1084-7980C>G
XM_011522203.1:c.1528C>G	XP_011520505.1:p.Arg510Gly
XM_011522203.2:c.1528C>G	XP_011520505.1:p.Arg510Gly
XM_011522204.1:c.1528C>G	XP_011520506.1:p.Arg510Gly
XM_011522204.3:c.1528C>G	XP_011520506.1:p.Arg510Gly
XM_011522205.1:c.1528C>G	XP_011520507.1:p.Arg510Gly
XM_011522205.3:c.1528C>G	XP_011520507.1:p.Arg510Gly
XM_011522206.1:c.1528C>G	XP_011520508.1:p.Arg510Gly
XM_011522206.3:c.1528C>G	XP_011520508.1:p.Arg510Gly
XM_011522207.1:c.1528C>G	XP_011520509.1:p.Arg510Gly
XM_011522208.1:c.1501C>G	XP_011520510.1:p.Arg501Gly
XM_011522208.3:c.1501C>G	XP_011520510.1:p.Arg501Gly
XM_011522209.1:c.1450C>G	XP_011520511.1:p.Arg484Gly
XM_011522209.2:c.1450C>G	XP_011520511.1:p.Arg484Gly
XM_011522210.1:c.1528C>G	XP_011520512.1:p.Arg510Gly
XM_011522210.2:c.1528C>G	XP_011520512.1:p.Arg510Gly
XM_011522211.1:c.1294C>G	XP_011520513.1:p.Arg432Gly
XM_011522211.3:c.1294C>G	XP_011520513.1:p.Arg432Gly
XM_011522212.1:c.1528C>G	XP_011520514.1:p.Arg510Gly
XM_011522213.1:c.1528C>G	XP_011520515.1:p.Arg510Gly
XM_011522214.1:c.1528C>G	XP_011520516.1:p.Arg510Gly
XM_011522214.2:c.1528C>G	XP_011520516.1:p.Arg510Gly
XM_011522215.1:c.1084-7980C>G	XP_011520517.1:n.1084-7980C>G
XM_011522215.2:c.1084-7980C>G	XP_011520517.1:n.1084-7980C>G
XM_011522216.1:c.1294C>G	XP_011520518.1:p.Arg432Gly
XM_011522216.2:c.1294C>G	XP_011520518.1:p.Arg432Gly
XM_011522217.1:c.1084-7980C>G	XP_011520519.1:n.1084-7980C>G
XM_017022723.1:c.1528C>G	XP_016878212.1:p.Arg510Gly
XM_024450099.1:c.1528C>G	XP_024305867.1:p.Arg510Gly
XM_024450100.1:c.1450C>G	XP_024305868.1:p.Arg484Gly
XM_024450101.1:c.1450C>G	XP_024305869.1:p.Arg484Gly
XM_024450102.1:c.487C>G	XP_024305870.1:p.Arg163Gly
XR_931944.1:n.1603C>G
XR_931944.2:n.1603C>G