Canonical Allele Identifier: CA1358940338

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39397031T= , CM000665.2:g.39397031T=	GRCh38
NC_000003.11:g.39438522T= , CM000665.1:g.39438522T=	GRCh37
NC_000003.10:g.39413526T=	NCBI36
NG_016931.1:g.18708T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648579.1:c.*723T=	ENSP00000497638.1:n.*723T=
ENST00000650617.1:c.*511T= MANE Select	ENSP00000497532.1:n.*511T=
ENST00000273158.8:c.*511T=	ENSP00000273158.3:n.*511T=
NM_017875.2:c.*511T=	NP_060345.2:n.*511T=
XM_006713214.1:c.*511T=	XP_006713277.1:n.*511T=
XM_011533869.1:c.*511T=	XP_011532171.1:n.*511T=
XM_011533870.1:c.*511T=	XP_011532172.1:n.*511T=
XM_011533871.1:c.*511T=	XP_011532173.1:n.*511T=
NM_001354798.1:c.*545T=	NP_001341727.1:n.*545T=
NM_017875.4:c.*511T= MANE Select	NP_060345.2:n.*511T=
XM_006713214.2:c.*511T=	XP_006713277.1:n.*511T=
XM_011533869.2:c.*511T=	XP_011532171.1:n.*511T=
XM_024453611.1:c.*511T=	XP_024309379.1:n.*511T=
NM_001354798.2:c.*545T=	NP_001341727.1:n.*545T=