Canonical Allele Identifier: CA433162430

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39391924C>A , CM000665.2:g.39391924C>A	GRCh38
NC_000003.11:g.39433415C>A , CM000665.1:g.39433415C>A	GRCh37
NC_000003.10:g.39408419C>A	NCBI36
NG_016931.1:g.13601C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_017875.4:c.528C>A MANE Select	NP_060345.2:p.Gly176=
ENST00000650617.1:c.528C>A MANE Select	ENSP00000497532.1:p.Gly176=
NM_001354798.1:c.528C>A	NP_001341727.1:p.Gly176=
NM_001354798.2:c.528C>A	NP_001341727.1:p.Gly176=
NM_017875.2:c.528C>A	NP_060345.2:p.Gly176=
ENST00000273158.8:c.528C>A	ENSP00000273158.3:p.Gly176=
ENST00000642683.1:c.480C>A	ENSP00000495376.1:p.Gly160=
ENST00000643672.1:c.477C>A	ENSP00000494532.1:p.Gly159=
ENST00000645280.1:c.474C>A	ENSP00000496690.1:p.Gly158=
ENST00000645630.1:c.348C>A	ENSP00000493714.1:p.Gly116=
ENST00000648579.1:c.528C>A	ENSP00000497638.1:p.Gly176=
XM_006713214.1:c.516C>A	XP_006713277.1:p.Gly172=
XM_006713214.2:c.516C>A	XP_006713277.1:p.Gly172=
XM_011533869.1:c.510C>A	XP_011532171.1:p.Gly170=
XM_011533869.2:c.510C>A	XP_011532171.1:p.Gly170=
XM_011533870.1:c.477C>A	XP_011532172.1:p.Gly159=
XM_011533871.1:c.348C>A	XP_011532173.1:p.Gly116=
XM_024453611.1:c.474C>A	XP_024309379.1:p.Gly158=