Canonical Allele Identifier: CA1358939311

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394514C= , CM000665.2:g.39394514C=	GRCh38
NC_000003.11:g.39436005C= , CM000665.1:g.39436005C=	GRCh37
NC_000003.10:g.39411009C=	NCBI36
NG_016931.1:g.16191C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.682C=	ENSP00000495376.1:p.His228=
ENST00000643672.1:c.679C=	ENSP00000494532.1:p.His227=
ENST00000645280.1:c.676C=	ENSP00000496690.1:p.His226=
ENST00000648579.1:c.*27C=	ENSP00000497638.1:n.*27C=
ENST00000650617.1:c.730C= MANE Select	ENSP00000497532.1:p.His244=
ENST00000273158.8:c.730C=	ENSP00000273158.3:p.His244=
NM_017875.2:c.730C=	NP_060345.2:p.His244=
XM_006713214.1:c.718C=	XP_006713277.1:p.His240=
XM_011533869.1:c.712C=	XP_011532171.1:p.His238=
XM_011533870.1:c.679C=	XP_011532172.1:p.His227=
XM_011533871.1:c.550C=	XP_011532173.1:p.His184=
NM_001354798.1:c.626-1884C=	NP_001341727.1:n.626-1884C=
NM_017875.4:c.730C= MANE Select	NP_060345.2:p.His244=
XM_006713214.2:c.718C=	XP_006713277.1:p.His240=
XM_011533869.2:c.712C=	XP_011532171.1:p.His238=
XM_024453611.1:c.676C=	XP_024309379.1:p.His226=
NM_001354798.2:c.626-1884C=	NP_001341727.1:n.626-1884C=