Canonical Allele Identifier: CA2327393

Gene: SLC25A38

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39390470C>G , CM000665.2:g.39390470C>G	GRCh38
NC_000003.11:g.39431961C>G , CM000665.1:g.39431961C>G	GRCh37
NC_000003.10:g.39406965C>G	NCBI36
NG_016931.1:g.12147C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642442.1:n.300C>G
ENST00000642683.1:c.228+11C>G	ENSP00000495376.1:n.228+11C>G
ENST00000642978.1:c.221C>G	ENSP00000494342.1:p.Thr74Arg
ENST00000643672.1:c.188C>G	ENSP00000494532.1:p.Thr63Arg
ENST00000645280.1:c.185C>G	ENSP00000496690.1:p.Thr62Arg
ENST00000645630.1:c.239C>G	ENSP00000493714.1:p.Thr80Arg
ENST00000648579.1:c.239C>G	ENSP00000497638.1:p.Thr80Arg
ENST00000650617.1:c.239C>G MANE Select	ENSP00000497532.1:p.Thr80Arg
ENST00000273158.8:c.239C>G	ENSP00000273158.3:p.Thr80Arg
ENST00000431510.1:c.227C>G	ENSP00000394244.1:p.Thr76Arg
NM_017875.2:c.239C>G	NP_060345.2:p.Thr80Arg
XM_006713214.1:c.227C>G	XP_006713277.1:p.Thr76Arg
XM_011533869.1:c.221C>G	XP_011532171.1:p.Thr74Arg
XM_011533870.1:c.188C>G	XP_011532172.1:p.Thr63Arg
XM_011533871.1:c.239C>G	XP_011532173.1:p.Thr80Arg
NM_001354798.1:c.239C>G	NP_001341727.1:p.Thr80Arg
NM_017875.4:c.239C>G MANE Select	NP_060345.2:p.Thr80Arg
XM_006713214.2:c.227C>G	XP_006713277.1:p.Thr76Arg
XM_011533869.2:c.221C>G	XP_011532171.1:p.Thr74Arg
XM_024453611.1:c.185C>G	XP_024309379.1:p.Thr62Arg
NM_001354798.2:c.239C>G	NP_001341727.1:p.Thr80Arg