Canonical Allele Identifier: CA2327453

Gene: SLC25A38

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39391630A>G , CM000665.2:g.39391630A>G	GRCh38
NC_000003.11:g.39433121A>G , CM000665.1:g.39433121A>G	GRCh37
NC_000003.10:g.39408125A>G	NCBI36
NG_016931.1:g.13307A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_017875.4:c.456+10A>G MANE Select	NP_060345.2:n.456+10A>G
ENST00000650617.1:c.456+10A>G MANE Select	ENSP00000497532.1:n.456+10A>G
NM_001354798.1:c.456+10A>G	NP_001341727.1:n.456+10A>G
NM_001354798.2:c.456+10A>G	NP_001341727.1:n.456+10A>G
NM_017875.2:c.456+10A>G	NP_060345.2:n.456+10A>G
ENST00000273158.8:c.456+10A>G	ENSP00000273158.3:n.456+10A>G
ENST00000642683.1:c.408+10A>G	ENSP00000495376.1:n.408+10A>G
ENST00000643672.1:c.405+10A>G	ENSP00000494532.1:n.405+10A>G
ENST00000645280.1:c.402+10A>G	ENSP00000496690.1:n.402+10A>G
ENST00000645630.1:c.277-223A>G	ENSP00000493714.1:n.277-223A>G
ENST00000648579.1:c.456+10A>G	ENSP00000497638.1:n.456+10A>G
XM_006713214.1:c.444+10A>G	XP_006713277.1:n.444+10A>G
XM_006713214.2:c.444+10A>G	XP_006713277.1:n.444+10A>G
XM_011533869.1:c.438+10A>G	XP_011532171.1:n.438+10A>G
XM_011533869.2:c.438+10A>G	XP_011532171.1:n.438+10A>G
XM_011533870.1:c.405+10A>G	XP_011532172.1:n.405+10A>G
XM_011533871.1:c.277-223A>G	XP_011532173.1:n.277-223A>G
XM_024453611.1:c.402+10A>G	XP_024309379.1:n.402+10A>G