Canonical Allele Identifier: CA345735072

Gene: TRAPPC12 TRAPPC12-AS1

Linked Data

• ClinVar Variation Id: 2237466
• ClinVar RCV Id: RCV002724041
• dbSNP Id: rs1666445385
• MyVariant Identifiers: chr2:g.3483117C>A (hg19) ; chr2:g.3479346C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3479346C>A , CM000664.2:g.3479346C>A	GRCh38
NC_000002.11:g.3483117C>A , CM000664.1:g.3483117C>A	GRCh37
NC_000002.10:g.3462124C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324266.10:c.2093C>A (TRAPPC12) MANE Select	ENSP00000324318.5:p.Thr698Asn
ENST00000324266.9:c.2093C>A (TRAPPC12)	ENSP00000324318.5:p.Thr698Asn
ENST00000382110.6:c.2093C>A (TRAPPC12)	ENSP00000371544.2:p.Thr698Asn
ENST00000415624.5:c.590C>A (TRAPPC12)	ENSP00000396592.1:p.Thr197Asn
ENST00000416918.5:c.252C>A (TRAPPC12)
ENST00000417243.5:c.826C>A (TRAPPC12)
ENST00000452495.1:c.169+413C>A (TRAPPC12)
ENST00000469400.1:n.499C>A (TRAPPC12)
ENST00000493792.1:n.348C>A (TRAPPC12)
ENST00000497597.5:n.3181C>A (TRAPPC12)
NM_016030.5:c.2093C>A (TRAPPC12)	NP_057114.5:p.Thr698Asn
XM_005264693.2:c.2093C>A (TRAPPC12)	XP_005264750.1:p.Thr698Asn
XM_011510350.1:c.1979C>A (TRAPPC12)	XP_011508652.1:p.Thr660Asn
XM_011510355.1:c.1148C>A (TRAPPC12)	XP_011508657.1:p.Thr383Asn
XM_011510356.1:c.1025C>A (TRAPPC12)	XP_011508658.1:p.Thr342Asn
XR_426956.2:n.2190C>A (TRAPPC12)
NM_001321102.1:c.2093C>A (TRAPPC12)	NP_001308031.1:p.Thr698Asn
XM_011510350.2:c.1979C>A (TRAPPC12)	XP_011508652.1:p.Thr660Asn
XM_011510355.2:c.1148C>A (TRAPPC12)	XP_011508657.1:p.Thr383Asn
XR_001738762.1:n.3213C>A (TRAPPC12)
XR_426956.3:n.2628C>A (TRAPPC12)
NM_016030.6:c.2093C>A (TRAPPC12) MANE Select	NP_057114.5:p.Thr698Asn
NM_001321102.2:c.2093C>A (TRAPPC12)	NP_001308031.1:p.Thr698Asn
NR_046720.1:n.3648G>T (TRAPPC12-AS1)