Canonical Allele Identifier: CA1358939271

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394414G= , CM000665.2:g.39394414G=	GRCh38
NC_000003.11:g.39435905G= , CM000665.1:g.39435905G=	GRCh37
NC_000003.10:g.39410909G=	NCBI36
NG_016931.1:g.16091G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.582G=	ENSP00000495376.1:p.Gln194=
ENST00000643672.1:c.579G=	ENSP00000494532.1:p.Gln193=
ENST00000645280.1:c.576G=	ENSP00000496690.1:p.Gln192=
ENST00000645630.1:c.450G=	ENSP00000493714.1:p.Gln150=
ENST00000648579.1:c.722-36G=	ENSP00000497638.1:n.722-36G=
ENST00000650617.1:c.630G= MANE Select	ENSP00000497532.1:p.Gln210=
ENST00000273158.8:c.630G=	ENSP00000273158.3:p.Gln210=
NM_017875.2:c.630G=	NP_060345.2:p.Gln210=
XM_006713214.1:c.618G=	XP_006713277.1:p.Gln206=
XM_011533869.1:c.612G=	XP_011532171.1:p.Gln204=
XM_011533870.1:c.579G=	XP_011532172.1:p.Gln193=
XM_011533871.1:c.450G=	XP_011532173.1:p.Gln150=
NM_001354798.1:c.626-1984G=	NP_001341727.1:n.626-1984G=
NM_017875.4:c.630G= MANE Select	NP_060345.2:p.Gln210=
XM_006713214.2:c.618G=	XP_006713277.1:p.Gln206=
XM_011533869.2:c.612G=	XP_011532171.1:p.Gln204=
XM_024453611.1:c.576G=	XP_024309379.1:p.Gln192=
NM_001354798.2:c.626-1984G=	NP_001341727.1:n.626-1984G=