Canonical Allele Identifier: CA1358939297

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394473_39394474delinsTG , CM000665.2:g.39394473_39394474delinsTG	GRCh38
NC_000003.11:g.39435964_39435965delinsTG , CM000665.1:g.39435964_39435965delinsTG	GRCh37
NC_000003.10:g.39410968_39410969delinsTG	NCBI36
NG_016931.1:g.16150_16151delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.641_642delinsTG	ENSP00000495376.1:p.Leu214=
ENST00000643672.1:c.638_639delinsTG	ENSP00000494532.1:p.Leu213=
ENST00000645280.1:c.635_636delinsTG	ENSP00000496690.1:p.Leu212=
ENST00000648579.1:c.745_746delinsTG	ENSP00000497638.1:p.Trp249=
ENST00000650617.1:c.689_690delinsTG MANE Select	ENSP00000497532.1:p.Leu230=
ENST00000273158.8:c.689_690delinsTG	ENSP00000273158.3:p.Leu230=
NM_017875.2:c.689_690delinsTG	NP_060345.2:p.Leu230=
XM_006713214.1:c.677_678delinsTG	XP_006713277.1:p.Leu226=
XM_011533869.1:c.671_672delinsTG	XP_011532171.1:p.Leu224=
XM_011533870.1:c.638_639delinsTG	XP_011532172.1:p.Leu213=
XM_011533871.1:c.509_510delinsTG	XP_011532173.1:p.Leu170=
NM_001354798.1:c.626-1925_626-1924delinsTG	NP_001341727.1:n.626-1925_626-1924delinsTG
NM_017875.4:c.689_690delinsTG MANE Select	NP_060345.2:p.Leu230=
XM_006713214.2:c.677_678delinsTG	XP_006713277.1:p.Leu226=
XM_011533869.2:c.671_672delinsTG	XP_011532171.1:p.Leu224=
XM_024453611.1:c.635_636delinsTG	XP_024309379.1:p.Leu212=
NM_001354798.2:c.626-1925_626-1924delinsTG	NP_001341727.1:n.626-1925_626-1924delinsTG