Canonical Allele Identifier: CA2327438

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39391546A>G , CM000665.2:g.39391546A>G	GRCh38
NC_000003.11:g.39433037A>G , CM000665.1:g.39433037A>G	GRCh37
NC_000003.10:g.39408041A>G	NCBI36
NG_016931.1:g.13223A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_017875.4:c.382A>G MANE Select	NP_060345.2:p.Met128Val
ENST00000650617.1:c.382A>G MANE Select	ENSP00000497532.1:p.Met128Val
NM_001354798.1:c.382A>G	NP_001341727.1:p.Met128Val
NM_001354798.2:c.382A>G	NP_001341727.1:p.Met128Val
NM_017875.2:c.382A>G	NP_060345.2:p.Met128Val
ENST00000273158.8:c.382A>G	ENSP00000273158.3:p.Met128Val
ENST00000431510.1:c.370A>G	ENSP00000394244.1:p.Met124Val
ENST00000642683.1:c.334A>G	ENSP00000495376.1:p.Met112Val
ENST00000643672.1:c.331A>G	ENSP00000494532.1:p.Met111Val
ENST00000645280.1:c.328A>G	ENSP00000496690.1:p.Met110Val
ENST00000645630.1:c.277-307A>G	ENSP00000493714.1:n.277-307A>G
ENST00000648579.1:c.382A>G	ENSP00000497638.1:p.Met128Val
XM_006713214.1:c.370A>G	XP_006713277.1:p.Met124Val
XM_006713214.2:c.370A>G	XP_006713277.1:p.Met124Val
XM_011533869.1:c.364A>G	XP_011532171.1:p.Met122Val
XM_011533869.2:c.364A>G	XP_011532171.1:p.Met122Val
XM_011533870.1:c.331A>G	XP_011532172.1:p.Met111Val
XM_011533871.1:c.277-307A>G	XP_011532173.1:n.277-307A>G
XM_024453611.1:c.328A>G	XP_024309379.1:p.Met110Val