Canonical Allele Identifier: CA1358939299

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394486A= , CM000665.2:g.39394486A=	GRCh38
NC_000003.11:g.39435977A= , CM000665.1:g.39435977A=	GRCh37
NC_000003.10:g.39410981A=	NCBI36
NG_016931.1:g.16163A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000642683.1:c.654A=	ENSP00000495376.1:p.Val218=
ENST00000643672.1:c.651A=	ENSP00000494532.1:p.Val217=
ENST00000645280.1:c.648A=	ENSP00000496690.1:p.Val216=
ENST00000648579.1:c.758A=	ENSP00000497638.1:p.Ter253=
ENST00000650617.1:c.702A= MANE Select	ENSP00000497532.1:p.Val234=
ENST00000273158.8:c.702A=	ENSP00000273158.3:p.Val234=
NM_017875.2:c.702A=	NP_060345.2:p.Val234=
XM_006713214.1:c.690A=	XP_006713277.1:p.Val230=
XM_011533869.1:c.684A=	XP_011532171.1:p.Val228=
XM_011533870.1:c.651A=	XP_011532172.1:p.Val217=
XM_011533871.1:c.522A=	XP_011532173.1:p.Val174=
NM_001354798.1:c.626-1912A=	NP_001341727.1:n.626-1912A=
NM_017875.4:c.702A= MANE Select	NP_060345.2:p.Val234=
XM_006713214.2:c.690A=	XP_006713277.1:p.Val230=
XM_011533869.2:c.684A=	XP_011532171.1:p.Val228=
XM_024453611.1:c.648A=	XP_024309379.1:p.Val216=
NM_001354798.2:c.626-1912A=	NP_001341727.1:n.626-1912A=