Canonical Allele Identifier: CA358874712

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183706872G>A , CM000666.2:g.183706872G>A	GRCh38
NC_000004.11:g.184628025G>A , CM000666.1:g.184628025G>A	GRCh37
NC_000004.10:g.184865019G>A	NCBI36
NG_033102.1:g.52606G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.3121G>A MANE Select	NP_068761.4:p.Asp1041Asn
ENST00000334690.11:c.3121G>A MANE Select	ENSP00000335371.6:p.Asp1041Asn
NM_021942.5:c.3121G>A	NP_068761.4:p.Asp1041Asn
NM_199053.2:c.3121G>A	NP_951008.1:p.Asp1041Asn
NM_199053.3:c.3121G>A	NP_951008.1:p.Asp1041Asn
ENST00000334690.10:c.3121G>A	ENSP00000335371.6:p.Asp1041Asn
ENST00000357207.8:c.3121G>A	ENSP00000349738.4:p.Asp1041Asn
ENST00000505676.5:c.*1235G>A	ENSP00000422915.1:n.*1235G>A
ENST00000506426.1:n.327G>A
ENST00000511955.5:n.1114G>A
ENST00000512476.1:c.1939G>A	ENSP00000421004.1:p.Asp647Asn
XM_024454179.1:c.3121G>A	XP_024309947.1:p.Asp1041Asn
XM_024454180.1:c.3121G>A	XP_024309948.1:p.Asp1041Asn
XM_024454181.1:c.1771G>A	XP_024309949.1:p.Asp591Asn
XR_001741315.2:n.3394G>A