Canonical Allele Identifier: CA352201218

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39391565G>A , CM000665.2:g.39391565G>A	GRCh38
NC_000003.11:g.39433056G>A , CM000665.1:g.39433056G>A	GRCh37
NC_000003.10:g.39408060G>A	NCBI36
NG_016931.1:g.13242G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_017875.4:c.401G>A MANE Select	NP_060345.2:p.Arg134His
ENST00000650617.1:c.401G>A MANE Select	ENSP00000497532.1:p.Arg134His
NM_001354798.1:c.401G>A	NP_001341727.1:p.Arg134His
NM_001354798.2:c.401G>A	NP_001341727.1:p.Arg134His
NM_017875.2:c.401G>A	NP_060345.2:p.Arg134His
ENST00000273158.8:c.401G>A	ENSP00000273158.3:p.Arg134His
ENST00000431510.1:c.389G>A	ENSP00000394244.1:p.Arg130His
ENST00000642683.1:c.353G>A	ENSP00000495376.1:p.Arg118His
ENST00000643672.1:c.350G>A	ENSP00000494532.1:p.Arg117His
ENST00000645280.1:c.347G>A	ENSP00000496690.1:p.Arg116His
ENST00000645630.1:c.277-288G>A	ENSP00000493714.1:n.277-288G>A
ENST00000648579.1:c.401G>A	ENSP00000497638.1:p.Arg134His
XM_006713214.1:c.389G>A	XP_006713277.1:p.Arg130His
XM_006713214.2:c.389G>A	XP_006713277.1:p.Arg130His
XM_011533869.1:c.383G>A	XP_011532171.1:p.Arg128His
XM_011533869.2:c.383G>A	XP_011532171.1:p.Arg128His
XM_011533870.1:c.350G>A	XP_011532172.1:p.Arg117His
XM_011533871.1:c.277-288G>A	XP_011532173.1:n.277-288G>A
XM_024453611.1:c.347G>A	XP_024309379.1:p.Arg116His