Canonical Allele Identifier: CA1358939334
Gene: SLC25A38 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39394574A= , CM000665.2:g.39394574A= GRCh38
NC_000003.11:g.39436065A= , CM000665.1:g.39436065A= GRCh37
NC_000003.10:g.39411069A= NCBI36
NG_016931.1:g.16251A=

Transcript Alleles

HGVS Amino-acid change
ENST00000642683.1:c.742A= ENSP00000495376.1:p.Lys248=
ENST00000643672.1:c.739A= ENSP00000494532.1:p.Lys247=
ENST00000645280.1:c.736A= ENSP00000496690.1:p.Lys246=
ENST00000648579.1:c.*87A= ENSP00000497638.1:n.*87A=
ENST00000650617.1:c.790A= MANE Select ENSP00000497532.1:p.Lys264=
ENST00000273158.8:c.790A= ENSP00000273158.3:p.Lys264=
NM_017875.2:c.790A= NP_060345.2:p.Lys264=
XM_006713214.1:c.778A= XP_006713277.1:p.Lys260=
XM_011533869.1:c.772A= XP_011532171.1:p.Lys258=
XM_011533870.1:c.739A= XP_011532172.1:p.Lys247=
XM_011533871.1:c.610A= XP_011532173.1:p.Lys204=
NM_001354798.1:c.626-1824A= NP_001341727.1:n.626-1824A=
NM_017875.4:c.790A= MANE Select NP_060345.2:p.Lys264=
XM_006713214.2:c.778A= XP_006713277.1:p.Lys260=
XM_011533869.2:c.772A= XP_011532171.1:p.Lys258=
XM_024453611.1:c.736A= XP_024309379.1:p.Lys246=
NM_001354798.2:c.626-1824A= NP_001341727.1:n.626-1824A=