Canonical Allele Identifier: CA2665163891

Gene: SLC25A38

Linked Data

• gnomAD v4: 3-39397012-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39397012A>G , CM000665.2:g.39397012A>G	GRCh38
NC_000003.11:g.39438503A>G , CM000665.1:g.39438503A>G	GRCh37
NC_000003.10:g.39413507A>G	NCBI36
NG_016931.1:g.18689A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643672.1:c.*492A>G	ENSP00000494532.1:n.*492A>G
ENST00000648579.1:c.*704A>G	ENSP00000497638.1:n.*704A>G
ENST00000650617.1:c.*492A>G MANE Select	ENSP00000497532.1:n.*492A>G
ENST00000273158.8:c.*492A>G	ENSP00000273158.3:n.*492A>G
NM_017875.2:c.*492A>G	NP_060345.2:n.*492A>G
XM_006713214.1:c.*492A>G	XP_006713277.1:n.*492A>G
XM_011533869.1:c.*492A>G	XP_011532171.1:n.*492A>G
XM_011533870.1:c.*492A>G	XP_011532172.1:n.*492A>G
XM_011533871.1:c.*492A>G	XP_011532173.1:n.*492A>G
NM_001354798.1:c.*526A>G	NP_001341727.1:n.*526A>G
NM_017875.4:c.*492A>G MANE Select	NP_060345.2:n.*492A>G
XM_006713214.2:c.*492A>G	XP_006713277.1:n.*492A>G
XM_011533869.2:c.*492A>G	XP_011532171.1:n.*492A>G
XM_024453611.1:c.*492A>G	XP_024309379.1:n.*492A>G
NM_001354798.2:c.*526A>G	NP_001341727.1:n.*526A>G