Canonical Allele Identifier: CA352205634

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436038A>G (hg19) ; chr3:g.39394547A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394547A>G , CM000665.2:g.39394547A>G	GRCh38
NC_000003.11:g.39436038A>G , CM000665.1:g.39436038A>G	GRCh37
NC_000003.10:g.39411042A>G	NCBI36
NG_016931.1:g.16224A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.715A>G	ENSP00000495376.1:p.Ile239Val
ENST00000643672.1:c.712A>G	ENSP00000494532.1:p.Ile238Val
ENST00000645280.1:c.709A>G	ENSP00000496690.1:p.Ile237Val
ENST00000648579.1:c.*60A>G	ENSP00000497638.1:n.*60A>G
ENST00000650617.1:c.763A>G MANE Select	ENSP00000497532.1:p.Ile255Val
ENST00000273158.8:c.763A>G	ENSP00000273158.3:p.Ile255Val
NM_017875.2:c.763A>G	NP_060345.2:p.Ile255Val
XM_006713214.1:c.751A>G	XP_006713277.1:p.Ile251Val
XM_011533869.1:c.745A>G	XP_011532171.1:p.Ile249Val
XM_011533870.1:c.712A>G	XP_011532172.1:p.Ile238Val
XM_011533871.1:c.583A>G	XP_011532173.1:p.Ile195Val
NM_001354798.1:c.626-1851A>G	NP_001341727.1:n.626-1851A>G
NM_017875.4:c.763A>G MANE Select	NP_060345.2:p.Ile255Val
XM_006713214.2:c.751A>G	XP_006713277.1:p.Ile251Val
XM_011533869.2:c.745A>G	XP_011532171.1:p.Ile249Val
XM_024453611.1:c.709A>G	XP_024309379.1:p.Ile237Val
NM_001354798.2:c.626-1851A>G	NP_001341727.1:n.626-1851A>G