Canonical Allele Identifier: CA352205093

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435972C>A (hg19) ; chr3:g.39394481C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394481C>A , CM000665.2:g.39394481C>A	GRCh38
NC_000003.11:g.39435972C>A , CM000665.1:g.39435972C>A	GRCh37
NC_000003.10:g.39410976C>A	NCBI36
NG_016931.1:g.16158C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642683.1:c.649C>A	ENSP00000495376.1:p.Leu217Met
ENST00000643672.1:c.646C>A	ENSP00000494532.1:p.Leu216Met
ENST00000645280.1:c.643C>A	ENSP00000496690.1:p.Leu215Met
ENST00000648579.1:c.753C>A	ENSP00000497638.1:p.His251Gln
ENST00000650617.1:c.697C>A MANE Select	ENSP00000497532.1:p.Leu233Met
ENST00000273158.8:c.697C>A	ENSP00000273158.3:p.Leu233Met
NM_017875.2:c.697C>A	NP_060345.2:p.Leu233Met
XM_006713214.1:c.685C>A	XP_006713277.1:p.Leu229Met
XM_011533869.1:c.679C>A	XP_011532171.1:p.Leu227Met
XM_011533870.1:c.646C>A	XP_011532172.1:p.Leu216Met
XM_011533871.1:c.517C>A	XP_011532173.1:p.Leu173Met
NM_001354798.1:c.626-1917C>A	NP_001341727.1:n.626-1917C>A
NM_017875.4:c.697C>A MANE Select	NP_060345.2:p.Leu233Met
XM_006713214.2:c.685C>A	XP_006713277.1:p.Leu229Met
XM_011533869.2:c.679C>A	XP_011532171.1:p.Leu227Met
XM_024453611.1:c.643C>A	XP_024309379.1:p.Leu215Met
NM_001354798.2:c.626-1917C>A	NP_001341727.1:n.626-1917C>A