Canonical Allele Identifier: CA445803932

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097056C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761356C>T , CM000667.2:g.110761356C>T	GRCh38
NC_000005.9:g.110097056C>T , CM000667.1:g.110097056C>T	GRCh37
NC_000005.8:g.110124955C>T	NCBI36
NG_051334.1:g.28221C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.831C>T MANE Select	ENSP00000348211.3:p.Ile277=
ENST00000355943.7:c.831C>T	ENSP00000348211.3:p.Ile277=
ENST00000447245.6:c.679-91C>T	ENSP00000399717.2:n.679-91C>T
ENST00000502462.6:n.1147C>T
ENST00000504098.1:c.393C>T	ENSP00000425708.1:p.Ile131=
ENST00000509432.1:c.192C>T	ENSP00000426604.1:p.Ile64=
ENST00000513706.2:n.2431C>T
ENST00000513807.5:c.345C>T	ENSP00000421134.1:p.Ile115=
NM_001303249.1:c.679-91C>T	NP_001290178.1:n.679-91C>T
NM_001303250.1:c.558C>T	NP_001290179.1:p.Ile186=
NM_138773.2:c.831C>T	NP_620128.1:p.Ile277=
NM_001303249.2:c.679-91C>T	NP_001290178.1:n.679-91C>T
NM_001303250.2:c.558C>T	NP_001290179.1:p.Ile186=
NM_138773.3:c.831C>T	NP_620128.1:p.Ile277=
NR_138151.1:n.1105C>T
NM_138773.4:c.831C>T MANE Select	NP_620128.1:p.Ile277=
NM_001303249.3:c.679-91C>T	NP_001290178.1:n.679-91C>T
NM_001303250.3:c.558C>T	NP_001290179.1:p.Ile186=
NR_138151.2:n.1070C>T