Canonical Allele Identifier: CA6732844

Gene: SLC25A3

Linked Data

• dbSNP Id: rs758319058
• ExAC: 12:98989187 AT / A
• gnomAD v2: 12-98989187-AT-A
• gnomAD v3: 12-98595409-AT-A
• gnomAD v4: 12-98595409-AT-A
• MyVariant Identifiers: chr12:g.98989189del (hg19) ; chr12:g.98989188del (hg19) ; chr12:g.98595410del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98595420del , CM000674.2:g.98595420del	GRCh38
NC_000012.11:g.98989198del , CM000674.1:g.98989198del	GRCh37
NC_000012.10:g.97513329del	NCBI36
NG_011702.1:g.6796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228318.8:c.158-13del MANE Plus Clinical	ENSP00000228318.3:n.158-13del
ENST00000552981.6:c.158-307del MANE Select	ENSP00000448708.2:n.158-307del
ENST00000188376.9:c.158-307del	ENSP00000188376.5:n.158-307del
ENST00000228318.7:c.158-13del	ENSP00000228318.3:n.158-13del
ENST00000401722.7:c.158-307del	ENSP00000383898.3:n.158-307del
ENST00000546766.5:n.1532del
ENST00000547534.5:c.158-307del	ENSP00000449793.1:n.158-307del
ENST00000548046.5:c.158-13del	ENSP00000447339.1:n.158-13del
ENST00000548847.1:c.158-307del	ENSP00000449166.1:n.158-307del
ENST00000549338.5:c.158-307del	ENSP00000447740.1:n.158-307del
ENST00000550695.1:c.158-13del	ENSP00000449479.1:n.158-13del
ENST00000551123.5:c.158-13del	ENSP00000449009.1:n.158-13del
ENST00000551917.5:c.158-13del	ENSP00000447310.1:n.158-13del
ENST00000552981.5:c.158-307del	ENSP00000448708.1:n.158-307del
NM_002635.3:c.158-307del	NP_002626.1:n.158-307del
NM_005888.3:c.158-13del	NP_005879.1:n.158-13del
NM_213611.2:c.158-307del	NP_998776.1:n.158-307del
NM_002635.4:c.158-307del MANE Select	NP_002626.1:n.158-307del
NM_213611.3:c.158-307del	NP_998776.1:n.158-307del
NM_005888.4:c.158-13del MANE Plus Clinical	NP_005879.1:n.158-13del