Canonical Allele Identifier: CA352205546

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436030T>A (hg19) ; chr3:g.39394539T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394539T>A , CM000665.2:g.39394539T>A	GRCh38
NC_000003.11:g.39436030T>A , CM000665.1:g.39436030T>A	GRCh37
NC_000003.10:g.39411034T>A	NCBI36
NG_016931.1:g.16216T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.707T>A	ENSP00000495376.1:p.Phe236Tyr
ENST00000643672.1:c.704T>A	ENSP00000494532.1:p.Phe235Tyr
ENST00000645280.1:c.701T>A	ENSP00000496690.1:p.Phe234Tyr
ENST00000648579.1:c.*52T>A	ENSP00000497638.1:n.*52T>A
ENST00000650617.1:c.755T>A MANE Select	ENSP00000497532.1:p.Phe252Tyr
ENST00000273158.8:c.755T>A	ENSP00000273158.3:p.Phe252Tyr
NM_017875.2:c.755T>A	NP_060345.2:p.Phe252Tyr
XM_006713214.1:c.743T>A	XP_006713277.1:p.Phe248Tyr
XM_011533869.1:c.737T>A	XP_011532171.1:p.Phe246Tyr
XM_011533870.1:c.704T>A	XP_011532172.1:p.Phe235Tyr
XM_011533871.1:c.575T>A	XP_011532173.1:p.Phe192Tyr
NM_001354798.1:c.626-1859T>A	NP_001341727.1:n.626-1859T>A
NM_017875.4:c.755T>A MANE Select	NP_060345.2:p.Phe252Tyr
XM_006713214.2:c.743T>A	XP_006713277.1:p.Phe248Tyr
XM_011533869.2:c.737T>A	XP_011532171.1:p.Phe246Tyr
XM_024453611.1:c.701T>A	XP_024309379.1:p.Phe234Tyr
NM_001354798.2:c.626-1859T>A	NP_001341727.1:n.626-1859T>A