Canonical Allele Identifier: CA1358939313

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394518T= , CM000665.2:g.39394518T=	GRCh38
NC_000003.11:g.39436009T= , CM000665.1:g.39436009T=	GRCh37
NC_000003.10:g.39411013T=	NCBI36
NG_016931.1:g.16195T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.686T=	ENSP00000495376.1:p.Met229=
ENST00000643672.1:c.683T=	ENSP00000494532.1:p.Met228=
ENST00000645280.1:c.680T=	ENSP00000496690.1:p.Met227=
ENST00000648579.1:c.*31T=	ENSP00000497638.1:n.*31T=
ENST00000650617.1:c.734T= MANE Select	ENSP00000497532.1:p.Met245=
ENST00000273158.8:c.734T=	ENSP00000273158.3:p.Met245=
NM_017875.2:c.734T=	NP_060345.2:p.Met245=
XM_006713214.1:c.722T=	XP_006713277.1:p.Met241=
XM_011533869.1:c.716T=	XP_011532171.1:p.Met239=
XM_011533870.1:c.683T=	XP_011532172.1:p.Met228=
XM_011533871.1:c.554T=	XP_011532173.1:p.Met185=
NM_001354798.1:c.626-1880T=	NP_001341727.1:n.626-1880T=
NM_017875.4:c.734T= MANE Select	NP_060345.2:p.Met245=
XM_006713214.2:c.722T=	XP_006713277.1:p.Met241=
XM_011533869.2:c.716T=	XP_011532171.1:p.Met239=
XM_024453611.1:c.680T=	XP_024309379.1:p.Met227=
NM_001354798.2:c.626-1880T=	NP_001341727.1:n.626-1880T=