Canonical Allele Identifier: CA352205616

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436036G>C (hg19) ; chr3:g.39394545G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394545G>C , CM000665.2:g.39394545G>C	GRCh38
NC_000003.11:g.39436036G>C , CM000665.1:g.39436036G>C	GRCh37
NC_000003.10:g.39411040G>C	NCBI36
NG_016931.1:g.16222G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.713G>C	ENSP00000495376.1:p.Trp238Ser
ENST00000643672.1:c.710G>C	ENSP00000494532.1:p.Trp237Ser
ENST00000645280.1:c.707G>C	ENSP00000496690.1:p.Trp236Ser
ENST00000648579.1:c.*58G>C	ENSP00000497638.1:n.*58G>C
ENST00000650617.1:c.761G>C MANE Select	ENSP00000497532.1:p.Trp254Ser
ENST00000273158.8:c.761G>C	ENSP00000273158.3:p.Trp254Ser
NM_017875.2:c.761G>C	NP_060345.2:p.Trp254Ser
XM_006713214.1:c.749G>C	XP_006713277.1:p.Trp250Ser
XM_011533869.1:c.743G>C	XP_011532171.1:p.Trp248Ser
XM_011533870.1:c.710G>C	XP_011532172.1:p.Trp237Ser
XM_011533871.1:c.581G>C	XP_011532173.1:p.Trp194Ser
NM_001354798.1:c.626-1853G>C	NP_001341727.1:n.626-1853G>C
NM_017875.4:c.761G>C MANE Select	NP_060345.2:p.Trp254Ser
XM_006713214.2:c.749G>C	XP_006713277.1:p.Trp250Ser
XM_011533869.2:c.743G>C	XP_011532171.1:p.Trp248Ser
XM_024453611.1:c.707G>C	XP_024309379.1:p.Trp236Ser
NM_001354798.2:c.626-1853G>C	NP_001341727.1:n.626-1853G>C