Canonical Allele Identifier: CA352205147

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435979C>T (hg19) ; chr3:g.39394488C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394488C>T , CM000665.2:g.39394488C>T	GRCh38
NC_000003.11:g.39435979C>T , CM000665.1:g.39435979C>T	GRCh37
NC_000003.10:g.39410983C>T	NCBI36
NG_016931.1:g.16165C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642683.1:c.656C>T	ENSP00000495376.1:p.Thr219Ile
ENST00000643672.1:c.653C>T	ENSP00000494532.1:p.Thr218Ile
ENST00000645280.1:c.650C>T	ENSP00000496690.1:p.Thr217Ile
ENST00000648579.1:c.*1C>T	ENSP00000497638.1:n.*1C>T
ENST00000650617.1:c.704C>T MANE Select	ENSP00000497532.1:p.Thr235Ile
ENST00000273158.8:c.704C>T	ENSP00000273158.3:p.Thr235Ile
NM_017875.2:c.704C>T	NP_060345.2:p.Thr235Ile
XM_006713214.1:c.692C>T	XP_006713277.1:p.Thr231Ile
XM_011533869.1:c.686C>T	XP_011532171.1:p.Thr229Ile
XM_011533870.1:c.653C>T	XP_011532172.1:p.Thr218Ile
XM_011533871.1:c.524C>T	XP_011532173.1:p.Thr175Ile
NM_001354798.1:c.626-1910C>T	NP_001341727.1:n.626-1910C>T
NM_017875.4:c.704C>T MANE Select	NP_060345.2:p.Thr235Ile
XM_006713214.2:c.692C>T	XP_006713277.1:p.Thr231Ile
XM_011533869.2:c.686C>T	XP_011532171.1:p.Thr229Ile
XM_024453611.1:c.650C>T	XP_024309379.1:p.Thr217Ile
NM_001354798.2:c.626-1910C>T	NP_001341727.1:n.626-1910C>T