Canonical Allele Identifier: CA352204384

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435903C>A (hg19) ; chr3:g.39394412C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394412C>A , CM000665.2:g.39394412C>A	GRCh38
NC_000003.11:g.39435903C>A , CM000665.1:g.39435903C>A	GRCh37
NC_000003.10:g.39410907C>A	NCBI36
NG_016931.1:g.16089C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.580C>A	ENSP00000495376.1:p.Gln194Lys
ENST00000643672.1:c.577C>A	ENSP00000494532.1:p.Gln193Lys
ENST00000645280.1:c.574C>A	ENSP00000496690.1:p.Gln192Lys
ENST00000645630.1:c.448C>A	ENSP00000493714.1:p.Gln150Lys
ENST00000648579.1:c.722-38C>A	ENSP00000497638.1:n.722-38C>A
ENST00000650617.1:c.628C>A MANE Select	ENSP00000497532.1:p.Gln210Lys
ENST00000273158.8:c.628C>A	ENSP00000273158.3:p.Gln210Lys
NM_017875.2:c.628C>A	NP_060345.2:p.Gln210Lys
XM_006713214.1:c.616C>A	XP_006713277.1:p.Gln206Lys
XM_011533869.1:c.610C>A	XP_011532171.1:p.Gln204Lys
XM_011533870.1:c.577C>A	XP_011532172.1:p.Gln193Lys
XM_011533871.1:c.448C>A	XP_011532173.1:p.Gln150Lys
NM_001354798.1:c.626-1986C>A	NP_001341727.1:n.626-1986C>A
NM_017875.4:c.628C>A MANE Select	NP_060345.2:p.Gln210Lys
XM_006713214.2:c.616C>A	XP_006713277.1:p.Gln206Lys
XM_011533869.2:c.610C>A	XP_011532171.1:p.Gln204Lys
XM_024453611.1:c.574C>A	XP_024309379.1:p.Gln192Lys
NM_001354798.2:c.626-1986C>A	NP_001341727.1:n.626-1986C>A