Canonical Allele Identifier: CA352205277

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435994T>C (hg19) ; chr3:g.39394503T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394503T>C , CM000665.2:g.39394503T>C	GRCh38
NC_000003.11:g.39435994T>C , CM000665.1:g.39435994T>C	GRCh37
NC_000003.10:g.39410998T>C	NCBI36
NG_016931.1:g.16180T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.671T>C	ENSP00000495376.1:p.Val224Ala
ENST00000643672.1:c.668T>C	ENSP00000494532.1:p.Val223Ala
ENST00000645280.1:c.665T>C	ENSP00000496690.1:p.Val222Ala
ENST00000648579.1:c.*16T>C	ENSP00000497638.1:n.*16T>C
ENST00000650617.1:c.719T>C MANE Select	ENSP00000497532.1:p.Val240Ala
ENST00000273158.8:c.719T>C	ENSP00000273158.3:p.Val240Ala
NM_017875.2:c.719T>C	NP_060345.2:p.Val240Ala
XM_006713214.1:c.707T>C	XP_006713277.1:p.Val236Ala
XM_011533869.1:c.701T>C	XP_011532171.1:p.Val234Ala
XM_011533870.1:c.668T>C	XP_011532172.1:p.Val223Ala
XM_011533871.1:c.539T>C	XP_011532173.1:p.Val180Ala
NM_001354798.1:c.626-1895T>C	NP_001341727.1:n.626-1895T>C
NM_017875.4:c.719T>C MANE Select	NP_060345.2:p.Val240Ala
XM_006713214.2:c.707T>C	XP_006713277.1:p.Val236Ala
XM_011533869.2:c.701T>C	XP_011532171.1:p.Val234Ala
XM_024453611.1:c.665T>C	XP_024309379.1:p.Val222Ala
NM_001354798.2:c.626-1895T>C	NP_001341727.1:n.626-1895T>C