Canonical Allele Identifier: CA433164993

Gene: SLC25A38

Linked Data

• dbSNP Id: rs2041808143
• MyVariant Identifiers: chr3:g.39436064C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394573C>T , CM000665.2:g.39394573C>T	GRCh38
NC_000003.11:g.39436064C>T , CM000665.1:g.39436064C>T	GRCh37
NC_000003.10:g.39411068C>T	NCBI36
NG_016931.1:g.16250C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.741C>T	ENSP00000495376.1:p.Phe247=
ENST00000643672.1:c.738C>T	ENSP00000494532.1:p.Phe246=
ENST00000645280.1:c.735C>T	ENSP00000496690.1:p.Phe245=
ENST00000648579.1:c.*86C>T	ENSP00000497638.1:n.*86C>T
ENST00000650617.1:c.789C>T MANE Select	ENSP00000497532.1:p.Phe263=
ENST00000273158.8:c.789C>T	ENSP00000273158.3:p.Phe263=
NM_017875.2:c.789C>T	NP_060345.2:p.Phe263=
XM_006713214.1:c.777C>T	XP_006713277.1:p.Phe259=
XM_011533869.1:c.771C>T	XP_011532171.1:p.Phe257=
XM_011533870.1:c.738C>T	XP_011532172.1:p.Phe246=
XM_011533871.1:c.609C>T	XP_011532173.1:p.Phe203=
NM_001354798.1:c.626-1825C>T	NP_001341727.1:n.626-1825C>T
NM_017875.4:c.789C>T MANE Select	NP_060345.2:p.Phe263=
XM_006713214.2:c.777C>T	XP_006713277.1:p.Phe259=
XM_011533869.2:c.771C>T	XP_011532171.1:p.Phe257=
XM_024453611.1:c.735C>T	XP_024309379.1:p.Phe245=
NM_001354798.2:c.626-1825C>T	NP_001341727.1:n.626-1825C>T