Canonical Allele Identifier: CA1358939331

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394568A= , CM000665.2:g.39394568A=	GRCh38
NC_000003.11:g.39436059A= , CM000665.1:g.39436059A=	GRCh37
NC_000003.10:g.39411063A=	NCBI36
NG_016931.1:g.16245A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.736A=	ENSP00000495376.1:p.Ile246=
ENST00000643672.1:c.733A=	ENSP00000494532.1:p.Ile245=
ENST00000645280.1:c.730A=	ENSP00000496690.1:p.Ile244=
ENST00000648579.1:c.*81A=	ENSP00000497638.1:n.*81A=
ENST00000650617.1:c.784A= MANE Select	ENSP00000497532.1:p.Ile262=
ENST00000273158.8:c.784A=	ENSP00000273158.3:p.Ile262=
NM_017875.2:c.784A=	NP_060345.2:p.Ile262=
XM_006713214.1:c.772A=	XP_006713277.1:p.Ile258=
XM_011533869.1:c.766A=	XP_011532171.1:p.Ile256=
XM_011533870.1:c.733A=	XP_011532172.1:p.Ile245=
XM_011533871.1:c.604A=	XP_011532173.1:p.Ile202=
NM_001354798.1:c.626-1830A=	NP_001341727.1:n.626-1830A=
NM_017875.4:c.784A= MANE Select	NP_060345.2:p.Ile262=
XM_006713214.2:c.772A=	XP_006713277.1:p.Ile258=
XM_011533869.2:c.766A=	XP_011532171.1:p.Ile256=
XM_024453611.1:c.730A=	XP_024309379.1:p.Ile244=
NM_001354798.2:c.626-1830A=	NP_001341727.1:n.626-1830A=