Canonical Allele Identifier: CA433164919

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436046A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394555A>G , CM000665.2:g.39394555A>G	GRCh38
NC_000003.11:g.39436046A>G , CM000665.1:g.39436046A>G	GRCh37
NC_000003.10:g.39411050A>G	NCBI36
NG_016931.1:g.16232A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.723A>G	ENSP00000495376.1:p.Gln241=
ENST00000643672.1:c.720A>G	ENSP00000494532.1:p.Gln240=
ENST00000645280.1:c.717A>G	ENSP00000496690.1:p.Gln239=
ENST00000648579.1:c.*68A>G	ENSP00000497638.1:n.*68A>G
ENST00000650617.1:c.771A>G MANE Select	ENSP00000497532.1:p.Gln257=
ENST00000273158.8:c.771A>G	ENSP00000273158.3:p.Gln257=
NM_017875.2:c.771A>G	NP_060345.2:p.Gln257=
XM_006713214.1:c.759A>G	XP_006713277.1:p.Gln253=
XM_011533869.1:c.753A>G	XP_011532171.1:p.Gln251=
XM_011533870.1:c.720A>G	XP_011532172.1:p.Gln240=
XM_011533871.1:c.591A>G	XP_011532173.1:p.Gln197=
NM_001354798.1:c.626-1843A>G	NP_001341727.1:n.626-1843A>G
NM_017875.4:c.771A>G MANE Select	NP_060345.2:p.Gln257=
XM_006713214.2:c.759A>G	XP_006713277.1:p.Gln253=
XM_011533869.2:c.753A>G	XP_011532171.1:p.Gln251=
XM_024453611.1:c.717A>G	XP_024309379.1:p.Gln239=
NM_001354798.2:c.626-1843A>G	NP_001341727.1:n.626-1843A>G