Canonical Allele Identifier: CA352205253

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435991A>T (hg19) ; chr3:g.39394500A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394500A>T , CM000665.2:g.39394500A>T	GRCh38
NC_000003.11:g.39435991A>T , CM000665.1:g.39435991A>T	GRCh37
NC_000003.10:g.39410995A>T	NCBI36
NG_016931.1:g.16177A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.668A>T	ENSP00000495376.1:p.Asp223Val
ENST00000643672.1:c.665A>T	ENSP00000494532.1:p.Asp222Val
ENST00000645280.1:c.662A>T	ENSP00000496690.1:p.Asp221Val
ENST00000648579.1:c.*13A>T	ENSP00000497638.1:n.*13A>T
ENST00000650617.1:c.716A>T MANE Select	ENSP00000497532.1:p.Asp239Val
ENST00000273158.8:c.716A>T	ENSP00000273158.3:p.Asp239Val
NM_017875.2:c.716A>T	NP_060345.2:p.Asp239Val
XM_006713214.1:c.704A>T	XP_006713277.1:p.Asp235Val
XM_011533869.1:c.698A>T	XP_011532171.1:p.Asp233Val
XM_011533870.1:c.665A>T	XP_011532172.1:p.Asp222Val
XM_011533871.1:c.536A>T	XP_011532173.1:p.Asp179Val
NM_001354798.1:c.626-1898A>T	NP_001341727.1:n.626-1898A>T
NM_017875.4:c.716A>T MANE Select	NP_060345.2:p.Asp239Val
XM_006713214.2:c.704A>T	XP_006713277.1:p.Asp235Val
XM_011533869.2:c.698A>T	XP_011532171.1:p.Asp233Val
XM_024453611.1:c.662A>T	XP_024309379.1:p.Asp221Val
NM_001354798.2:c.626-1898A>T	NP_001341727.1:n.626-1898A>T