Canonical Allele Identifier: CA352205668

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436042G>T (hg19) ; chr3:g.39394551G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394551G>T , CM000665.2:g.39394551G>T	GRCh38
NC_000003.11:g.39436042G>T , CM000665.1:g.39436042G>T	GRCh37
NC_000003.10:g.39411046G>T	NCBI36
NG_016931.1:g.16228G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.719G>T	ENSP00000495376.1:p.Gly240Val
ENST00000643672.1:c.716G>T	ENSP00000494532.1:p.Gly239Val
ENST00000645280.1:c.713G>T	ENSP00000496690.1:p.Gly238Val
ENST00000648579.1:c.*64G>T	ENSP00000497638.1:n.*64G>T
ENST00000650617.1:c.767G>T MANE Select	ENSP00000497532.1:p.Gly256Val
ENST00000273158.8:c.767G>T	ENSP00000273158.3:p.Gly256Val
NM_017875.2:c.767G>T	NP_060345.2:p.Gly256Val
XM_006713214.1:c.755G>T	XP_006713277.1:p.Gly252Val
XM_011533869.1:c.749G>T	XP_011532171.1:p.Gly250Val
XM_011533870.1:c.716G>T	XP_011532172.1:p.Gly239Val
XM_011533871.1:c.587G>T	XP_011532173.1:p.Gly196Val
NM_001354798.1:c.626-1847G>T	NP_001341727.1:n.626-1847G>T
NM_017875.4:c.767G>T MANE Select	NP_060345.2:p.Gly256Val
XM_006713214.2:c.755G>T	XP_006713277.1:p.Gly252Val
XM_011533869.2:c.749G>T	XP_011532171.1:p.Gly250Val
XM_024453611.1:c.713G>T	XP_024309379.1:p.Gly238Val
NM_001354798.2:c.626-1847G>T	NP_001341727.1:n.626-1847G>T