Canonical Allele Identifier: CA388151000

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48562821G>A (hg19) ; chr13:g.47988686G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988686G>A , CM000675.2:g.47988686G>A	GRCh38
NC_000013.10:g.48562821G>A , CM000675.1:g.48562821G>A	GRCh37
NC_000013.9:g.47460822G>A	NCBI36
NG_008241.1:g.17642C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.215C>T	ENSP00000495674.1:p.Ala72Val
ENST00000643023.1:c.389C>T	ENSP00000495664.1:p.Ala130Val
ENST00000643584.1:c.389C>T	ENSP00000494987.1:p.Ala130Val
ENST00000644338.1:c.389C>T	ENSP00000494723.1:p.Ala130Val
ENST00000646602.1:c.389C>T	ENSP00000495250.1:p.Ala130Val
ENST00000646804.1:c.215C>T	ENSP00000493977.1:p.Ala72Val
ENST00000646932.1:c.389C>T MANE Select	ENSP00000494360.1:p.Ala130Val
ENST00000647361.1:c.*182C>T	ENSP00000494607.1:n.*182C>T
ENST00000378654.8:c.389C>T	ENSP00000367923.3:p.Ala130Val
ENST00000433022.1:c.90+12494C>T	ENSP00000415091.1:n.90+12494C>T
ENST00000434484.5:c.179C>T	ENSP00000392771.1:p.Ala60Val
ENST00000470760.2:c.389C>T	ENSP00000488974.1:p.Ala130Val
ENST00000497202.6:c.483C>T	ENSP00000489175.1:n.483C>T
NM_003850.2:c.389C>T	NP_003841.1:p.Ala130Val
XM_011535292.1:c.152C>T	XP_011533594.1:p.Ala51Val
XM_011535293.1:c.-14C>T	XP_011533595.1:n.-14C>T
XR_941688.1:n.433C>T
NM_003850.3:c.389C>T MANE Select	NP_003841.1:p.Ala130Val