Canonical Allele Identifier: CA352205651

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39436041G>T (hg19) ; chr3:g.39394550G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394550G>T , CM000665.2:g.39394550G>T	GRCh38
NC_000003.11:g.39436041G>T , CM000665.1:g.39436041G>T	GRCh37
NC_000003.10:g.39411045G>T	NCBI36
NG_016931.1:g.16227G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642683.1:c.718G>T	ENSP00000495376.1:p.Gly240Cys
ENST00000643672.1:c.715G>T	ENSP00000494532.1:p.Gly239Cys
ENST00000645280.1:c.712G>T	ENSP00000496690.1:p.Gly238Cys
ENST00000648579.1:c.*63G>T	ENSP00000497638.1:n.*63G>T
ENST00000650617.1:c.766G>T MANE Select	ENSP00000497532.1:p.Gly256Cys
ENST00000273158.8:c.766G>T	ENSP00000273158.3:p.Gly256Cys
NM_017875.2:c.766G>T	NP_060345.2:p.Gly256Cys
XM_006713214.1:c.754G>T	XP_006713277.1:p.Gly252Cys
XM_011533869.1:c.748G>T	XP_011532171.1:p.Gly250Cys
XM_011533870.1:c.715G>T	XP_011532172.1:p.Gly239Cys
XM_011533871.1:c.586G>T	XP_011532173.1:p.Gly196Cys
NM_001354798.1:c.626-1848G>T	NP_001341727.1:n.626-1848G>T
NM_017875.4:c.766G>T MANE Select	NP_060345.2:p.Gly256Cys
XM_006713214.2:c.754G>T	XP_006713277.1:p.Gly252Cys
XM_011533869.2:c.748G>T	XP_011532171.1:p.Gly250Cys
XM_024453611.1:c.712G>T	XP_024309379.1:p.Gly238Cys
NM_001354798.2:c.626-1848G>T	NP_001341727.1:n.626-1848G>T