Canonical Allele Identifier: CA352205640

Gene: SLC25A38

Linked Data

• dbSNP Id: rs2041807869
• gnomAD v4: 3-39394548-T-C
• MyVariant Identifiers: chr3:g.39436039T>C (hg19) ; chr3:g.39394548T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394548T>C , CM000665.2:g.39394548T>C	GRCh38
NC_000003.11:g.39436039T>C , CM000665.1:g.39436039T>C	GRCh37
NC_000003.10:g.39411043T>C	NCBI36
NG_016931.1:g.16225T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.716T>C	ENSP00000495376.1:p.Ile239Thr
ENST00000643672.1:c.713T>C	ENSP00000494532.1:p.Ile238Thr
ENST00000645280.1:c.710T>C	ENSP00000496690.1:p.Ile237Thr
ENST00000648579.1:c.*61T>C	ENSP00000497638.1:n.*61T>C
ENST00000650617.1:c.764T>C MANE Select	ENSP00000497532.1:p.Ile255Thr
ENST00000273158.8:c.764T>C	ENSP00000273158.3:p.Ile255Thr
NM_017875.2:c.764T>C	NP_060345.2:p.Ile255Thr
XM_006713214.1:c.752T>C	XP_006713277.1:p.Ile251Thr
XM_011533869.1:c.746T>C	XP_011532171.1:p.Ile249Thr
XM_011533870.1:c.713T>C	XP_011532172.1:p.Ile238Thr
XM_011533871.1:c.584T>C	XP_011532173.1:p.Ile195Thr
NM_001354798.1:c.626-1850T>C	NP_001341727.1:n.626-1850T>C
NM_017875.4:c.764T>C MANE Select	NP_060345.2:p.Ile255Thr
XM_006713214.2:c.752T>C	XP_006713277.1:p.Ile251Thr
XM_011533869.2:c.746T>C	XP_011532171.1:p.Ile249Thr
XM_024453611.1:c.710T>C	XP_024309379.1:p.Ile237Thr
NM_001354798.2:c.626-1850T>C	NP_001341727.1:n.626-1850T>C