Canonical Allele Identifier: CA2674823578

Gene: SLC25A46

Linked Data

• gnomAD v4: 5-110761112-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761112G>T , CM000667.2:g.110761112G>T	GRCh38
NC_000005.9:g.110096812G>T , CM000667.1:g.110096812G>T	GRCh37
NC_000005.8:g.110124711G>T	NCBI36
NG_051334.1:g.27977G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.679-92G>T MANE Select	ENSP00000348211.3:n.679-92G>T
ENST00000355943.7:c.679-92G>T	ENSP00000348211.3:n.679-92G>T
ENST00000447245.6:c.679-335G>T	ENSP00000399717.2:n.679-335G>T
ENST00000502462.6:n.995-92G>T
ENST00000504098.1:c.241-92G>T	ENSP00000425708.1:n.241-92G>T
ENST00000509432.1:c.40-92G>T	ENSP00000426604.1:n.40-92G>T
ENST00000513706.2:n.2279-92G>T
ENST00000513807.5:c.193-92G>T	ENSP00000421134.1:n.193-92G>T
NM_001303249.1:c.679-335G>T	NP_001290178.1:n.679-335G>T
NM_001303250.1:c.406-92G>T	NP_001290179.1:n.406-92G>T
NM_138773.2:c.679-92G>T	NP_620128.1:n.679-92G>T
NM_001303249.2:c.679-335G>T	NP_001290178.1:n.679-335G>T
NM_001303250.2:c.406-92G>T	NP_001290179.1:n.406-92G>T
NM_138773.3:c.679-92G>T	NP_620128.1:n.679-92G>T
NR_138151.1:n.953-92G>T
NM_138773.4:c.679-92G>T MANE Select	NP_620128.1:n.679-92G>T
NM_001303249.3:c.679-335G>T	NP_001290178.1:n.679-335G>T
NM_001303250.3:c.406-92G>T	NP_001290179.1:n.406-92G>T
NR_138151.2:n.918-92G>T