Canonical Allele Identifier: CA2327551

Gene: SLC25A38

Linked Data

• dbSNP Id: rs375346031
• ExAC: 3:39436107 A / C
• gnomAD v2: 3-39436107-A-C
• gnomAD v3: 3-39394616-A-C
• gnomAD v4: 3-39394616-A-C
• MyVariant Identifiers: chr3:g.39436107A>C (hg19) ; chr3:g.39394616A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39394616A>C , CM000665.2:g.39394616A>C	GRCh38
NC_000003.11:g.39436107A>C , CM000665.1:g.39436107A>C	GRCh37
NC_000003.10:g.39411111A>C	NCBI36
NG_016931.1:g.16293A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643672.1:c.741+40A>C	ENSP00000494532.1:n.741+40A>C
ENST00000645280.1:c.738+40A>C	ENSP00000496690.1:n.738+40A>C
ENST00000648579.1:c.*89+40A>C	ENSP00000497638.1:n.*89+40A>C
ENST00000650617.1:c.792+40A>C MANE Select	ENSP00000497532.1:n.792+40A>C
ENST00000273158.8:c.792+40A>C	ENSP00000273158.3:n.792+40A>C
NM_017875.2:c.792+40A>C	NP_060345.2:n.792+40A>C
XM_006713214.1:c.780+40A>C	XP_006713277.1:n.780+40A>C
XM_011533869.1:c.774+40A>C	XP_011532171.1:n.774+40A>C
XM_011533870.1:c.741+40A>C	XP_011532172.1:n.741+40A>C
XM_011533871.1:c.612+40A>C	XP_011532173.1:n.612+40A>C
NM_001354798.1:c.626-1782A>C	NP_001341727.1:n.626-1782A>C
NM_017875.4:c.792+40A>C MANE Select	NP_060345.2:n.792+40A>C
XM_006713214.2:c.780+40A>C	XP_006713277.1:n.780+40A>C
XM_011533869.2:c.774+40A>C	XP_011532171.1:n.774+40A>C
XM_024453611.1:c.738+40A>C	XP_024309379.1:n.738+40A>C
NM_001354798.2:c.626-1782A>C	NP_001341727.1:n.626-1782A>C