Canonical Allele Identifier: CA352205064

Gene: SLC25A38

Linked Data

• MyVariant Identifiers: chr3:g.39435969T>A (hg19) ; chr3:g.39394478T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394478T>A , CM000665.2:g.39394478T>A	GRCh38
NC_000003.11:g.39435969T>A , CM000665.1:g.39435969T>A	GRCh37
NC_000003.10:g.39410973T>A	NCBI36
NG_016931.1:g.16155T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642683.1:c.646T>A	ENSP00000495376.1:p.Ser216Thr
ENST00000643672.1:c.643T>A	ENSP00000494532.1:p.Ser215Thr
ENST00000645280.1:c.640T>A	ENSP00000496690.1:p.Ser214Thr
ENST00000648579.1:c.750T>A	ENSP00000497638.1:p.Pro250=
ENST00000650617.1:c.694T>A MANE Select	ENSP00000497532.1:p.Ser232Thr
ENST00000273158.8:c.694T>A	ENSP00000273158.3:p.Ser232Thr
NM_017875.2:c.694T>A	NP_060345.2:p.Ser232Thr
XM_006713214.1:c.682T>A	XP_006713277.1:p.Ser228Thr
XM_011533869.1:c.676T>A	XP_011532171.1:p.Ser226Thr
XM_011533870.1:c.643T>A	XP_011532172.1:p.Ser215Thr
XM_011533871.1:c.514T>A	XP_011532173.1:p.Ser172Thr
NM_001354798.1:c.626-1920T>A	NP_001341727.1:n.626-1920T>A
NM_017875.4:c.694T>A MANE Select	NP_060345.2:p.Ser232Thr
XM_006713214.2:c.682T>A	XP_006713277.1:p.Ser228Thr
XM_011533869.2:c.676T>A	XP_011532171.1:p.Ser226Thr
XM_024453611.1:c.640T>A	XP_024309379.1:p.Ser214Thr
NM_001354798.2:c.626-1920T>A	NP_001341727.1:n.626-1920T>A