Canonical Allele Identifier: CA609573030

Gene: SUCLA2

Linked Data

• gnomAD v2: 13-48563144-T-TTAGATGAGATAAAATTTTGGCTATTATGTGGATTTGCTTTTTCTCAACTG
• MyVariant Identifiers: chr13:g.48563144_48563145insTAGATGAGATAAAATTTTGGCTATTATGTGGATTTGCTTTTTCTCAACTG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.47989009_47989010insTAGATGAGATAAAATTTTGGCTATTATGTGGATTTGCTTTTTCTCAACTG , CM000675.2:g.47989009_47989010insTAGATGAGATAAAATTTTGGCTATTATGTGGATTTGCTTTTTCTCAACTG	GRCh38
NC_000013.10:g.48563144_48563145insTAGATGAGATAAAATTTTGGCTATTATGTGGATTTGCTTTTTCTCAACTG , CM000675.1:g.48563144_48563145insTAGATGAGATAAAATTTTGGCTATTATGTGGATTTGCTTTTTCTCAACTG	GRCh37
NC_000013.9:g.47461145_47461146insTAGATGAGATAAAATTTTGGCTATTATGTGGATTTGCTTTTTCTCAACTG	NCBI36
NG_008241.1:g.17318_17319insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642944.1:c.98-29_98-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000495674.1:n.98-29_98-28insCAGTTGAGAAAAAGCAAATCCACATAA...
ENST00000643023.1:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000495664.1:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACAT...
ENST00000643584.1:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000494987.1:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACAT...
ENST00000644338.1:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000494723.1:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACAT...
ENST00000646602.1:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000495250.1:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACAT...
ENST00000646804.1:c.98-29_98-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000493977.1:n.98-29_98-28insCAGTTGAGAAAAAGCAAATCCACATAA...
ENST00000646932.1:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA MANE Select	ENSP00000494360.1:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACAT...
ENST00000647361.1:c.*65-29_*65-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000494607.1:n.*65-29_*65-28insCAGTTGAGAAAAAGCAAATCCACAT...
ENST00000378654.8:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000367923.3:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACAT...
ENST00000433022.1:c.90+12170_90+12171insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000415091.1:n.90+12170_90+12171insCAGTTGAGAAAAAGCAAATCC...
ENST00000434484.5:c.62-29_62-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000392771.1:n.62-29_62-28insCAGTTGAGAAAAAGCAAATCCACATAA...
ENST00000470760.2:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000488974.1:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACAT...
ENST00000497202.6:c.366-29_366-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	ENSP00000489175.1:n.366-29_366-28insCAGTTGAGAAAAAGCAAATCCACAT...
NM_003850.2:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	NP_003841.1:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGC...
XM_011535292.1:c.35-29_35-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	XP_011533594.1:n.35-29_35-28insCAGTTGAGAAAAAGCAAATCCACATAATAG...
XM_011535293.1:c.-131-29_-131-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA	XP_011533595.1:n.-131-29_-131-28insCAGTTGAGAAAAAGCAAATCCACATA...
XR_941688.1:n.316-29_316-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA
NM_003850.3:c.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGCCAAAATTTTATCTCATCTA MANE Select	NP_003841.1:n.272-29_272-28insCAGTTGAGAAAAAGCAAATCCACATAATAGC...