Canonical Allele Identifier: CA442579698

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183694669T>C , CM000666.2:g.183694669T>C	GRCh38
NC_000004.11:g.184615822T>C , CM000666.1:g.184615822T>C	GRCh37
NC_000004.10:g.184852816T>C	NCBI36
NG_033102.1:g.40403T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.2574T>C MANE Select	NP_068761.4:p.Ser858=
ENST00000334690.11:c.2574T>C MANE Select	ENSP00000335371.6:p.Ser858=
NM_021942.5:c.2574T>C	NP_068761.4:p.Ser858=
NM_199053.2:c.2574T>C	NP_951008.1:p.Ser858=
NM_199053.3:c.2574T>C	NP_951008.1:p.Ser858=
ENST00000334690.10:c.2574T>C	ENSP00000335371.6:p.Ser858=
ENST00000357207.8:c.2574T>C	ENSP00000349738.4:p.Ser858=
ENST00000505676.5:c.*688T>C	ENSP00000422915.1:n.*688T>C
ENST00000512476.1:c.1392T>C	ENSP00000421004.1:p.Ser464=
XM_011532180.1:c.2574T>C	XP_011530482.1:p.Ser858=
XM_017008537.2:c.2574T>C	XP_016864026.1:p.Ser858=
XM_017008538.2:c.2574T>C	XP_016864027.1:p.Ser858=
XM_024454179.1:c.2574T>C	XP_024309947.1:p.Ser858=
XM_024454180.1:c.2574T>C	XP_024309948.1:p.Ser858=
XM_024454181.1:c.1224T>C	XP_024309949.1:p.Ser408=
XR_001741315.2:n.2766T>C