Canonical Allele Identifier: CA1358939308

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394510A= , CM000665.2:g.39394510A=	GRCh38
NC_000003.11:g.39436001A= , CM000665.1:g.39436001A=	GRCh37
NC_000003.10:g.39411005A=	NCBI36
NG_016931.1:g.16187A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.678A=	ENSP00000495376.1:p.Lys226=
ENST00000643672.1:c.675A=	ENSP00000494532.1:p.Lys225=
ENST00000645280.1:c.672A=	ENSP00000496690.1:p.Lys224=
ENST00000648579.1:c.*23A=	ENSP00000497638.1:n.*23A=
ENST00000650617.1:c.726A= MANE Select	ENSP00000497532.1:p.Lys242=
ENST00000273158.8:c.726A=	ENSP00000273158.3:p.Lys242=
NM_017875.2:c.726A=	NP_060345.2:p.Lys242=
XM_006713214.1:c.714A=	XP_006713277.1:p.Lys238=
XM_011533869.1:c.708A=	XP_011532171.1:p.Lys236=
XM_011533870.1:c.675A=	XP_011532172.1:p.Lys225=
XM_011533871.1:c.546A=	XP_011532173.1:p.Lys182=
NM_001354798.1:c.626-1888A=	NP_001341727.1:n.626-1888A=
NM_017875.4:c.726A= MANE Select	NP_060345.2:p.Lys242=
XM_006713214.2:c.714A=	XP_006713277.1:p.Lys238=
XM_011533869.2:c.708A=	XP_011532171.1:p.Lys236=
XM_024453611.1:c.672A=	XP_024309379.1:p.Lys224=
NM_001354798.2:c.626-1888A=	NP_001341727.1:n.626-1888A=