Canonical Allele Identifier: CA1358940278

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39396910C= , CM000665.2:g.39396910C=	GRCh38
NC_000003.11:g.39438401C= , CM000665.1:g.39438401C=	GRCh37
NC_000003.10:g.39413405C=	NCBI36
NG_016931.1:g.18587C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643672.1:c.*390C=	ENSP00000494532.1:n.*390C=
ENST00000648579.1:c.*602C=	ENSP00000497638.1:n.*602C=
ENST00000650617.1:c.*390C= MANE Select	ENSP00000497532.1:n.*390C=
ENST00000273158.8:c.*390C=	ENSP00000273158.3:n.*390C=
NM_017875.2:c.*390C=	NP_060345.2:n.*390C=
XM_006713214.1:c.*390C=	XP_006713277.1:n.*390C=
XM_011533869.1:c.*390C=	XP_011532171.1:n.*390C=
XM_011533870.1:c.*390C=	XP_011532172.1:n.*390C=
XM_011533871.1:c.*390C=	XP_011532173.1:n.*390C=
NM_001354798.1:c.*424C=	NP_001341727.1:n.*424C=
NM_017875.4:c.*390C= MANE Select	NP_060345.2:n.*390C=
XM_006713214.2:c.*390C=	XP_006713277.1:n.*390C=
XM_011533869.2:c.*390C=	XP_011532171.1:n.*390C=
XM_024453611.1:c.*390C=	XP_024309379.1:n.*390C=
NM_001354798.2:c.*424C=	NP_001341727.1:n.*424C=