Canonical Allele Identifier: CA3152223

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183694625C>A , CM000666.2:g.183694625C>A	GRCh38
NC_000004.11:g.184615778C>A , CM000666.1:g.184615778C>A	GRCh37
NC_000004.10:g.184852772C>A	NCBI36
NG_033102.1:g.40359C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.2530C>A MANE Select	NP_068761.4:p.Arg844Ser
ENST00000334690.11:c.2530C>A MANE Select	ENSP00000335371.6:p.Arg844Ser
NM_021942.5:c.2530C>A	NP_068761.4:p.Arg844Ser
NM_199053.2:c.2530C>A	NP_951008.1:p.Arg844Ser
NM_199053.3:c.2530C>A	NP_951008.1:p.Arg844Ser
ENST00000334690.10:c.2530C>A	ENSP00000335371.6:p.Arg844Ser
ENST00000357207.8:c.2530C>A	ENSP00000349738.4:p.Arg844Ser
ENST00000505676.5:c.*644C>A	ENSP00000422915.1:n.*644C>A
ENST00000512476.1:c.1348C>A	ENSP00000421004.1:p.Arg450Ser
XM_011532180.1:c.2530C>A	XP_011530482.1:p.Arg844Ser
XM_017008537.2:c.2530C>A	XP_016864026.1:p.Arg844Ser
XM_017008538.2:c.2530C>A	XP_016864027.1:p.Arg844Ser
XM_024454179.1:c.2530C>A	XP_024309947.1:p.Arg844Ser
XM_024454180.1:c.2530C>A	XP_024309948.1:p.Arg844Ser
XM_024454181.1:c.1180C>A	XP_024309949.1:p.Arg394Ser
XR_001741315.2:n.2722C>A