Canonical Allele Identifier: CA2564189442

Gene: SLC52A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.763660_763661insCATTAA , CM000682.2:g.763660_763661insCATTAA	GRCh38
NC_000020.10:g.744304_744305insCATTAA , CM000682.1:g.744304_744305insCATTAA	GRCh37
NC_000020.9:g.692304_692305insCATTAA	NCBI36
NG_027687.1:g.9924_9925insTTAATG
NG_027687.2:g.17325_17326insTTAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381944.5:c.910_911insTTAATG	ENSP00000371370.3:p.Tyr304delinsPheAsnAsp
ENST00000473664.2:c.567+1547_567+1548insTTAATG	ENSP00000502741.1:n.567+1547_567+1548insTTAATG
ENST00000488495.3:c.910_911insTTAATG	ENSP00000494009.1:p.Tyr304delinsPheAsnAsp
ENST00000645534.1:c.910_911insTTAATG MANE Select	ENSP00000494193.1:p.Tyr304delinsPheAsnAsp
ENST00000675066.1:c.910_911insTTAATG	ENSP00000501902.1:p.Tyr304delinsPheAsnAsp
ENST00000217254.11:c.910_911insTTAATG	ENSP00000217254.7:p.Tyr304delinsPheAsnAsp
ENST00000381944.4:c.910_911insTTAATG	ENSP00000371370.3:p.Tyr304delinsPheAsnAsp
ENST00000473664.1:n.618+1547_618+1548insTTAATG
ENST00000632431.1:c.910_911insTTAATG	ENSP00000488723.1:p.Tyr304delinsPheAsnAsp
NM_033409.3:c.910_911insTTAATG	NP_212134.3:p.Tyr304delinsPheAsnAsp
XM_005260655.3:c.910_911insTTAATG	XP_005260712.1:p.Tyr304delinsPheAsnAsp
XM_011529148.1:c.910_911insTTAATG	XP_011527450.1:p.Tyr304delinsPheAsnAsp
XM_005260655.4:c.910_911insTTAATG	XP_005260712.1:p.Tyr304delinsPheAsnAsp
XM_024451821.1:c.910_911insTTAATG	XP_024307589.1:p.Tyr304delinsPheAsnAsp
NM_033409.4:c.910_911insTTAATG MANE Select	NP_212134.3:p.Tyr304delinsPheAsnAsp
NM_001370085.1:c.910_911insTTAATG	NP_001357014.1:p.Tyr304delinsPheAsnAsp
NM_001370086.1:c.910_911insTTAATG	NP_001357015.1:p.Tyr304delinsPheAsnAsp