Canonical Allele Identifier: CA358861774

Gene: TRAPPC11

Linked Data

• ClinVar Variation Id: 541345
• ClinVar RCV Id: RCV000651606
• dbSNP Id: rs1554007706
• MyVariant Identifiers: chr4:g.184598609A>G (hg19) ; chr4:g.183677456A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183677456A>G , CM000666.2:g.183677456A>G	GRCh38
NC_000004.11:g.184598609A>G , CM000666.1:g.184598609A>G	GRCh37
NC_000004.10:g.184835603A>G	NCBI36
NG_033102.1:g.23190A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334690.11:c.735-2A>G MANE Select	ENSP00000335371.6:n.735-2A>G
ENST00000334690.10:c.735-2A>G	ENSP00000335371.6:n.735-2A>G
ENST00000357207.8:c.735-2A>G	ENSP00000349738.4:n.735-2A>G
ENST00000505676.5:c.163-2752A>G	ENSP00000422915.1:n.163-2752A>G
ENST00000511409.1:n.488-2A>G
ENST00000513600.5:n.528-2A>G
NM_021942.5:c.735-2A>G	NP_068761.4:n.735-2A>G
NM_199053.2:c.735-2A>G	NP_951008.1:n.735-2A>G
XM_011532180.1:c.735-2A>G	XP_011530482.1:n.735-2A>G
XM_017008537.2:c.735-2A>G	XP_016864026.1:n.735-2A>G
XM_017008538.2:c.735-2A>G	XP_016864027.1:n.735-2A>G
XM_024454179.1:c.735-2A>G	XP_024309947.1:n.735-2A>G
XM_024454180.1:c.735-2A>G	XP_024309948.1:n.735-2A>G
XM_024454181.1:c.-522-2A>G	XP_024309949.1:n.-522-2A>G
XR_001741315.2:n.927-2A>G
NM_021942.6:c.735-2A>G MANE Select	NP_068761.4:n.735-2A>G
NM_199053.3:c.735-2A>G	NP_951008.1:n.735-2A>G