Canonical Allele Identifier: CA352204364

Gene: SLC25A38

Linked Data

• gnomAD v4: 3-39394410-A-G
• MyVariant Identifiers: chr3:g.39435901A>G (hg19) ; chr3:g.39394410A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394410A>G , CM000665.2:g.39394410A>G	GRCh38
NC_000003.11:g.39435901A>G , CM000665.1:g.39435901A>G	GRCh37
NC_000003.10:g.39410905A>G	NCBI36
NG_016931.1:g.16087A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.578A>G	ENSP00000495376.1:p.Asp193Gly
ENST00000643672.1:c.575A>G	ENSP00000494532.1:p.Asp192Gly
ENST00000645280.1:c.572A>G	ENSP00000496690.1:p.Asp191Gly
ENST00000645630.1:c.446A>G	ENSP00000493714.1:p.Asp149Gly
ENST00000648579.1:c.722-40A>G	ENSP00000497638.1:n.722-40A>G
ENST00000650617.1:c.626A>G MANE Select	ENSP00000497532.1:p.Asp209Gly
ENST00000273158.8:c.626A>G	ENSP00000273158.3:p.Asp209Gly
NM_017875.2:c.626A>G	NP_060345.2:p.Asp209Gly
XM_006713214.1:c.614A>G	XP_006713277.1:p.Asp205Gly
XM_011533869.1:c.608A>G	XP_011532171.1:p.Asp203Gly
XM_011533870.1:c.575A>G	XP_011532172.1:p.Asp192Gly
XM_011533871.1:c.446A>G	XP_011532173.1:p.Asp149Gly
NM_001354798.1:c.626-1988A>G	NP_001341727.1:n.626-1988A>G
NM_017875.4:c.626A>G MANE Select	NP_060345.2:p.Asp209Gly
XM_006713214.2:c.614A>G	XP_006713277.1:p.Asp205Gly
XM_011533869.2:c.608A>G	XP_011532171.1:p.Asp203Gly
XM_024453611.1:c.572A>G	XP_024309379.1:p.Asp191Gly
NM_001354798.2:c.626-1988A>G	NP_001341727.1:n.626-1988A>G