Canonical Allele Identifier: CA1358939302

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394496G= , CM000665.2:g.39394496G=	GRCh38
NC_000003.11:g.39435987G= , CM000665.1:g.39435987G=	GRCh37
NC_000003.10:g.39410991G=	NCBI36
NG_016931.1:g.16173G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.664G=	ENSP00000495376.1:p.Ala222=
ENST00000643672.1:c.661G=	ENSP00000494532.1:p.Ala221=
ENST00000645280.1:c.658G=	ENSP00000496690.1:p.Ala220=
ENST00000648579.1:c.*9G=	ENSP00000497638.1:n.*9G=
ENST00000650617.1:c.712G= MANE Select	ENSP00000497532.1:p.Ala238=
ENST00000273158.8:c.712G=	ENSP00000273158.3:p.Ala238=
NM_017875.2:c.712G=	NP_060345.2:p.Ala238=
XM_006713214.1:c.700G=	XP_006713277.1:p.Ala234=
XM_011533869.1:c.694G=	XP_011532171.1:p.Ala232=
XM_011533870.1:c.661G=	XP_011532172.1:p.Ala221=
XM_011533871.1:c.532G=	XP_011532173.1:p.Ala178=
NM_001354798.1:c.626-1902G=	NP_001341727.1:n.626-1902G=
NM_017875.4:c.712G= MANE Select	NP_060345.2:p.Ala238=
XM_006713214.2:c.700G=	XP_006713277.1:p.Ala234=
XM_011533869.2:c.694G=	XP_011532171.1:p.Ala232=
XM_024453611.1:c.658G=	XP_024309379.1:p.Ala220=
NM_001354798.2:c.626-1902G=	NP_001341727.1:n.626-1902G=