Canonical Allele Identifier: CA433164527

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435968C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394477C>T , CM000665.2:g.39394477C>T	GRCh38
NC_000003.11:g.39435968C>T , CM000665.1:g.39435968C>T	GRCh37
NC_000003.10:g.39410972C>T	NCBI36
NG_016931.1:g.16154C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642683.1:c.645C>T	ENSP00000495376.1:p.Ala215=
ENST00000643672.1:c.642C>T	ENSP00000494532.1:p.Ala214=
ENST00000645280.1:c.639C>T	ENSP00000496690.1:p.Ala213=
ENST00000648579.1:c.749C>T	ENSP00000497638.1:p.Pro250Leu
ENST00000650617.1:c.693C>T MANE Select	ENSP00000497532.1:p.Ala231=
ENST00000273158.8:c.693C>T	ENSP00000273158.3:p.Ala231=
NM_017875.2:c.693C>T	NP_060345.2:p.Ala231=
XM_006713214.1:c.681C>T	XP_006713277.1:p.Ala227=
XM_011533869.1:c.675C>T	XP_011532171.1:p.Ala225=
XM_011533870.1:c.642C>T	XP_011532172.1:p.Ala214=
XM_011533871.1:c.513C>T	XP_011532173.1:p.Ala171=
NM_001354798.1:c.626-1921C>T	NP_001341727.1:n.626-1921C>T
NM_017875.4:c.693C>T MANE Select	NP_060345.2:p.Ala231=
XM_006713214.2:c.681C>T	XP_006713277.1:p.Ala227=
XM_011533869.2:c.675C>T	XP_011532171.1:p.Ala225=
XM_024453611.1:c.639C>T	XP_024309379.1:p.Ala213=
NM_001354798.2:c.626-1921C>T	NP_001341727.1:n.626-1921C>T