Canonical Allele Identifier: CA352201067

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39391552G>C , CM000665.2:g.39391552G>C	GRCh38
NC_000003.11:g.39433043G>C , CM000665.1:g.39433043G>C	GRCh37
NC_000003.10:g.39408047G>C	NCBI36
NG_016931.1:g.13229G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_017875.4:c.388G>C MANE Select	NP_060345.2:p.Gly130Arg
ENST00000650617.1:c.388G>C MANE Select	ENSP00000497532.1:p.Gly130Arg
NM_001354798.1:c.388G>C	NP_001341727.1:p.Gly130Arg
NM_001354798.2:c.388G>C	NP_001341727.1:p.Gly130Arg
NM_017875.2:c.388G>C	NP_060345.2:p.Gly130Arg
ENST00000273158.8:c.388G>C	ENSP00000273158.3:p.Gly130Arg
ENST00000431510.1:c.376G>C	ENSP00000394244.1:p.Gly126Arg
ENST00000642683.1:c.340G>C	ENSP00000495376.1:p.Gly114Arg
ENST00000643672.1:c.337G>C	ENSP00000494532.1:p.Gly113Arg
ENST00000645280.1:c.334G>C	ENSP00000496690.1:p.Gly112Arg
ENST00000645630.1:c.277-301G>C	ENSP00000493714.1:n.277-301G>C
ENST00000648579.1:c.388G>C	ENSP00000497638.1:p.Gly130Arg
XM_006713214.1:c.376G>C	XP_006713277.1:p.Gly126Arg
XM_006713214.2:c.376G>C	XP_006713277.1:p.Gly126Arg
XM_011533869.1:c.370G>C	XP_011532171.1:p.Gly124Arg
XM_011533869.2:c.370G>C	XP_011532171.1:p.Gly124Arg
XM_011533870.1:c.337G>C	XP_011532172.1:p.Gly113Arg
XM_011533871.1:c.277-301G>C	XP_011532173.1:n.277-301G>C
XM_024453611.1:c.334G>C	XP_024309379.1:p.Gly112Arg