Canonical Allele Identifier: CA1358939274

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394419A= , CM000665.2:g.39394419A=	GRCh38
NC_000003.11:g.39435910A= , CM000665.1:g.39435910A=	GRCh37
NC_000003.10:g.39410914A=	NCBI36
NG_016931.1:g.16096A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.587A=	ENSP00000495376.1:p.Asp196=
ENST00000643672.1:c.584A=	ENSP00000494532.1:p.Asp195=
ENST00000645280.1:c.581A=	ENSP00000496690.1:p.Asp194=
ENST00000648579.1:c.722-31A=	ENSP00000497638.1:n.722-31A=
ENST00000650617.1:c.635A= MANE Select	ENSP00000497532.1:p.Asp212=
ENST00000273158.8:c.635A=	ENSP00000273158.3:p.Asp212=
NM_017875.2:c.635A=	NP_060345.2:p.Asp212=
XM_006713214.1:c.623A=	XP_006713277.1:p.Asp208=
XM_011533869.1:c.617A=	XP_011532171.1:p.Asp206=
XM_011533870.1:c.584A=	XP_011532172.1:p.Asp195=
XM_011533871.1:c.455A=	XP_011532173.1:p.Asp152=
NM_001354798.1:c.626-1979A=	NP_001341727.1:n.626-1979A=
NM_017875.4:c.635A= MANE Select	NP_060345.2:p.Asp212=
XM_006713214.2:c.623A=	XP_006713277.1:p.Asp208=
XM_011533869.2:c.617A=	XP_011532171.1:p.Asp206=
XM_024453611.1:c.581A=	XP_024309379.1:p.Asp194=
NM_001354798.2:c.626-1979A=	NP_001341727.1:n.626-1979A=