Canonical Allele Identifier: CA388151296

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48563032A>G (hg19) ; chr13:g.47988897A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47988897A>G , CM000675.2:g.47988897A>G	GRCh38
NC_000013.10:g.48563032A>G , CM000675.1:g.48563032A>G	GRCh37
NC_000013.9:g.47461033A>G	NCBI36
NG_008241.1:g.17431T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.182T>C	ENSP00000495674.1:p.Val61Ala
ENST00000643023.1:c.356T>C	ENSP00000495664.1:p.Val119Ala
ENST00000643584.1:c.356T>C	ENSP00000494987.1:p.Val119Ala
ENST00000644338.1:c.356T>C	ENSP00000494723.1:p.Val119Ala
ENST00000646602.1:c.356T>C	ENSP00000495250.1:p.Val119Ala
ENST00000646804.1:c.182T>C	ENSP00000493977.1:p.Val61Ala
ENST00000646932.1:c.356T>C MANE Select	ENSP00000494360.1:p.Val119Ala
ENST00000647361.1:c.*149T>C	ENSP00000494607.1:n.*149T>C
ENST00000378654.8:c.356T>C	ENSP00000367923.3:p.Val119Ala
ENST00000433022.1:c.90+12283T>C	ENSP00000415091.1:n.90+12283T>C
ENST00000434484.5:c.146T>C	ENSP00000392771.1:p.Val49Ala
ENST00000470760.2:c.356T>C	ENSP00000488974.1:p.Val119Ala
ENST00000497202.6:c.450T>C	ENSP00000489175.1:n.450T>C
NM_003850.2:c.356T>C	NP_003841.1:p.Val119Ala
XM_011535292.1:c.119T>C	XP_011533594.1:p.Val40Ala
XM_011535293.1:c.-47T>C	XP_011533595.1:n.-47T>C
XR_941688.1:n.400T>C
NM_003850.3:c.356T>C MANE Select	NP_003841.1:p.Val119Ala