Canonical Allele Identifier: CA352205156
Gene: SLC25A38 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39394491A>T , CM000665.2:g.39394491A>T GRCh38
NC_000003.11:g.39435982A>T , CM000665.1:g.39435982A>T GRCh37
NC_000003.10:g.39410986A>T NCBI36
NG_016931.1:g.16168A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642683.1:c.659A>T ENSP00000495376.1:p.Gln220Leu
ENST00000643672.1:c.656A>T ENSP00000494532.1:p.Gln219Leu
ENST00000645280.1:c.653A>T ENSP00000496690.1:p.Gln218Leu
ENST00000648579.1:c.*4A>T ENSP00000497638.1:n.*4A>T
ENST00000650617.1:c.707A>T MANE Select ENSP00000497532.1:p.Gln236Leu
ENST00000273158.8:c.707A>T ENSP00000273158.3:p.Gln236Leu
NM_017875.2:c.707A>T NP_060345.2:p.Gln236Leu
XM_006713214.1:c.695A>T XP_006713277.1:p.Gln232Leu
XM_011533869.1:c.689A>T XP_011532171.1:p.Gln230Leu
XM_011533870.1:c.656A>T XP_011532172.1:p.Gln219Leu
XM_011533871.1:c.527A>T XP_011532173.1:p.Gln176Leu
NM_001354798.1:c.626-1907A>T NP_001341727.1:n.626-1907A>T
NM_017875.4:c.707A>T MANE Select NP_060345.2:p.Gln236Leu
XM_006713214.2:c.695A>T XP_006713277.1:p.Gln232Leu
XM_011533869.2:c.689A>T XP_011532171.1:p.Gln230Leu
XM_024453611.1:c.653A>T XP_024309379.1:p.Gln218Leu
NM_001354798.2:c.626-1907A>T NP_001341727.1:n.626-1907A>T