Canonical Allele Identifier: CA1358939306

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394506T= , CM000665.2:g.39394506T=	GRCh38
NC_000003.11:g.39435997T= , CM000665.1:g.39435997T=	GRCh37
NC_000003.10:g.39411001T=	NCBI36
NG_016931.1:g.16183T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.674T=	ENSP00000495376.1:p.Ile225=
ENST00000643672.1:c.671T=	ENSP00000494532.1:p.Ile224=
ENST00000645280.1:c.668T=	ENSP00000496690.1:p.Ile223=
ENST00000648579.1:c.*19T=	ENSP00000497638.1:n.*19T=
ENST00000650617.1:c.722T= MANE Select	ENSP00000497532.1:p.Ile241=
ENST00000273158.8:c.722T=	ENSP00000273158.3:p.Ile241=
NM_017875.2:c.722T=	NP_060345.2:p.Ile241=
XM_006713214.1:c.710T=	XP_006713277.1:p.Ile237=
XM_011533869.1:c.704T=	XP_011532171.1:p.Ile235=
XM_011533870.1:c.671T=	XP_011532172.1:p.Ile224=
XM_011533871.1:c.542T=	XP_011532173.1:p.Ile181=
NM_001354798.1:c.626-1892T=	NP_001341727.1:n.626-1892T=
NM_017875.4:c.722T= MANE Select	NP_060345.2:p.Ile241=
XM_006713214.2:c.710T=	XP_006713277.1:p.Ile237=
XM_011533869.2:c.704T=	XP_011532171.1:p.Ile235=
XM_024453611.1:c.668T=	XP_024309379.1:p.Ile223=
NM_001354798.2:c.626-1892T=	NP_001341727.1:n.626-1892T=