Canonical Allele Identifier: CA1358939333

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394573C= , CM000665.2:g.39394573C=	GRCh38
NC_000003.11:g.39436064C= , CM000665.1:g.39436064C=	GRCh37
NC_000003.10:g.39411068C=	NCBI36
NG_016931.1:g.16250C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.741C=	ENSP00000495376.1:p.Phe247=
ENST00000643672.1:c.738C=	ENSP00000494532.1:p.Phe246=
ENST00000645280.1:c.735C=	ENSP00000496690.1:p.Phe245=
ENST00000648579.1:c.*86C=	ENSP00000497638.1:n.*86C=
ENST00000650617.1:c.789C= MANE Select	ENSP00000497532.1:p.Phe263=
ENST00000273158.8:c.789C=	ENSP00000273158.3:p.Phe263=
NM_017875.2:c.789C=	NP_060345.2:p.Phe263=
XM_006713214.1:c.777C=	XP_006713277.1:p.Phe259=
XM_011533869.1:c.771C=	XP_011532171.1:p.Phe257=
XM_011533870.1:c.738C=	XP_011532172.1:p.Phe246=
XM_011533871.1:c.609C=	XP_011532173.1:p.Phe203=
NM_001354798.1:c.626-1825C=	NP_001341727.1:n.626-1825C=
NM_017875.4:c.789C= MANE Select	NP_060345.2:p.Phe263=
XM_006713214.2:c.777C=	XP_006713277.1:p.Phe259=
XM_011533869.2:c.771C=	XP_011532171.1:p.Phe257=
XM_024453611.1:c.735C=	XP_024309379.1:p.Phe245=
NM_001354798.2:c.626-1825C=	NP_001341727.1:n.626-1825C=