Canonical Allele Identifier: CA360697397

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097345A>G (hg19) ; chr5:g.110761645A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761645A>G , CM000667.2:g.110761645A>G	GRCh38
NC_000005.9:g.110097345A>G , CM000667.1:g.110097345A>G	GRCh37
NC_000005.8:g.110125244A>G	NCBI36
NG_051334.1:g.28510A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1120A>G MANE Select	ENSP00000348211.3:p.Asn374Asp
ENST00000355943.7:c.1120A>G	ENSP00000348211.3:p.Asn374Asp
ENST00000447245.6:c.877A>G	ENSP00000399717.2:p.Asn293Asp
ENST00000502462.6:n.1436A>G
ENST00000504098.1:c.682A>G	ENSP00000425708.1:p.Asn228Asp
ENST00000509432.1:c.481A>G	ENSP00000426604.1:p.Asn161Asp
ENST00000513706.2:n.2720A>G
ENST00000513807.5:c.634A>G	ENSP00000421134.1:p.Asn212Asp
NM_001303249.1:c.877A>G	NP_001290178.1:p.Asn293Asp
NM_001303250.1:c.847A>G	NP_001290179.1:p.Asn283Asp
NM_138773.2:c.1120A>G	NP_620128.1:p.Asn374Asp
NM_001303249.2:c.877A>G	NP_001290178.1:p.Asn293Asp
NM_001303250.2:c.847A>G	NP_001290179.1:p.Asn283Asp
NM_138773.3:c.1120A>G	NP_620128.1:p.Asn374Asp
NR_138151.1:n.1394A>G
NM_138773.4:c.1120A>G MANE Select	NP_620128.1:p.Asn374Asp
NM_001303249.3:c.877A>G	NP_001290178.1:p.Asn293Asp
NM_001303250.3:c.847A>G	NP_001290179.1:p.Asn283Asp
NR_138151.2:n.1359A>G