Canonical Allele Identifier: CA388249628

Gene: SUCLA2

Linked Data

• MyVariant Identifiers: chr13:g.48523635A>T (hg19) ; chr13:g.47949500A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47949500A>T , CM000675.2:g.47949500A>T	GRCh38
NC_000013.10:g.48523635A>T , CM000675.1:g.48523635A>T	GRCh37
NC_000013.9:g.47421636A>T	NCBI36
NG_008241.1:g.56828T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634878.2:c.724T>A
ENST00000642944.1:c.1037T>A	ENSP00000495674.1:p.Val346Asp
ENST00000643023.1:c.1274T>A	ENSP00000495664.1:p.Val425Asp
ENST00000643584.1:c.1211T>A	ENSP00000494987.1:p.Val404Asp
ENST00000646804.1:c.1037T>A	ENSP00000493977.1:p.Val346Asp
ENST00000646932.1:c.1211T>A MANE Select	ENSP00000494360.1:p.Val404Asp
ENST00000647361.1:c.*1004T>A	ENSP00000494607.1:n.*1004T>A
ENST00000378654.8:c.1211T>A	ENSP00000367923.3:p.Val404Asp
ENST00000467222.1:n.519T>A
ENST00000493152.6:c.62T>A	ENSP00000489055.1:p.Val21Asp
ENST00000634878.1:c.724T>A
NM_003850.2:c.1211T>A	NP_003841.1:p.Val404Asp
XM_011535292.1:c.974T>A	XP_011533594.1:p.Val325Asp
XM_011535293.1:c.809T>A	XP_011533595.1:p.Val270Asp
NM_003850.3:c.1211T>A MANE Select	NP_003841.1:p.Val404Asp