Canonical Allele Identifier: CA1358939261
Gene: SLC25A38 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39394383C= , CM000665.2:g.39394383C= GRCh38
NC_000003.11:g.39435874C= , CM000665.1:g.39435874C= GRCh37
NC_000003.10:g.39410878C= NCBI36
NG_016931.1:g.16060C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000642683.1:c.578-27C= ENSP00000495376.1:n.578-27C=
ENST00000643672.1:c.575-27C= ENSP00000494532.1:n.575-27C=
ENST00000645280.1:c.572-27C= ENSP00000496690.1:n.572-27C=
ENST00000645630.1:c.446-27C= ENSP00000493714.1:n.446-27C=
ENST00000648579.1:c.722-67C= ENSP00000497638.1:n.722-67C=
ENST00000650617.1:c.626-27C= MANE Select ENSP00000497532.1:n.626-27C=
ENST00000273158.8:c.626-27C= ENSP00000273158.3:n.626-27C=
NM_017875.2:c.626-27C= NP_060345.2:n.626-27C=
XM_006713214.1:c.614-27C= XP_006713277.1:n.614-27C=
XM_011533869.1:c.608-27C= XP_011532171.1:n.608-27C=
XM_011533870.1:c.575-27C= XP_011532172.1:n.575-27C=
XM_011533871.1:c.446-27C= XP_011532173.1:n.446-27C=
NM_001354798.1:c.626-2015C= NP_001341727.1:n.626-2015C=
NM_017875.4:c.626-27C= MANE Select NP_060345.2:n.626-27C=
XM_006713214.2:c.614-27C= XP_006713277.1:n.614-27C=
XM_011533869.2:c.608-27C= XP_011532171.1:n.608-27C=
XM_024453611.1:c.572-27C= XP_024309379.1:n.572-27C=
NM_001354798.2:c.626-2015C= NP_001341727.1:n.626-2015C=