Canonical Allele Identifier: CA1358939264
Gene: SLC25A38 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39394390T= , CM000665.2:g.39394390T= GRCh38
NC_000003.11:g.39435881T= , CM000665.1:g.39435881T= GRCh37
NC_000003.10:g.39410885T= NCBI36
NG_016931.1:g.16067T=

Transcript Alleles

HGVS Amino-acid change
ENST00000642683.1:c.578-20T= ENSP00000495376.1:n.578-20T=
ENST00000643672.1:c.575-20T= ENSP00000494532.1:n.575-20T=
ENST00000645280.1:c.572-20T= ENSP00000496690.1:n.572-20T=
ENST00000645630.1:c.446-20T= ENSP00000493714.1:n.446-20T=
ENST00000648579.1:c.722-60T= ENSP00000497638.1:n.722-60T=
ENST00000650617.1:c.626-20T= MANE Select ENSP00000497532.1:n.626-20T=
ENST00000273158.8:c.626-20T= ENSP00000273158.3:n.626-20T=
NM_017875.2:c.626-20T= NP_060345.2:n.626-20T=
XM_006713214.1:c.614-20T= XP_006713277.1:n.614-20T=
XM_011533869.1:c.608-20T= XP_011532171.1:n.608-20T=
XM_011533870.1:c.575-20T= XP_011532172.1:n.575-20T=
XM_011533871.1:c.446-20T= XP_011532173.1:n.446-20T=
NM_001354798.1:c.626-2008T= NP_001341727.1:n.626-2008T=
NM_017875.4:c.626-20T= MANE Select NP_060345.2:n.626-20T=
XM_006713214.2:c.614-20T= XP_006713277.1:n.614-20T=
XM_011533869.2:c.608-20T= XP_011532171.1:n.608-20T=
XM_024453611.1:c.572-20T= XP_024309379.1:n.572-20T=
NM_001354798.2:c.626-2008T= NP_001341727.1:n.626-2008T=