Canonical Allele Identifier: CA358867540

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183684796C>T , CM000666.2:g.183684796C>T	GRCh38
NC_000004.11:g.184605949C>T , CM000666.1:g.184605949C>T	GRCh37
NC_000004.10:g.184842943C>T	NCBI36
NG_033102.1:g.30530C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.1522C>T MANE Select	NP_068761.4:p.Gln508Ter
ENST00000334690.11:c.1522C>T MANE Select	ENSP00000335371.6:p.Gln508Ter
NM_021942.5:c.1522C>T	NP_068761.4:p.Gln508Ter
NM_199053.2:c.1522C>T	NP_951008.1:p.Gln508Ter
NM_199053.3:c.1522C>T	NP_951008.1:p.Gln508Ter
ENST00000334690.10:c.1522C>T	ENSP00000335371.6:p.Gln508Ter
ENST00000357207.8:c.1522C>T	ENSP00000349738.4:p.Gln508Ter
ENST00000505676.5:c.348+790C>T	ENSP00000422915.1:n.348+790C>T
ENST00000512476.1:c.340C>T	ENSP00000421004.1:p.Gln114Ter
XM_011532180.1:c.1522C>T	XP_011530482.1:p.Gln508Ter
XM_017008537.2:c.1522C>T	XP_016864026.1:p.Gln508Ter
XM_017008538.2:c.1522C>T	XP_016864027.1:p.Gln508Ter
XM_024454179.1:c.1522C>T	XP_024309947.1:p.Gln508Ter
XM_024454180.1:c.1522C>T	XP_024309948.1:p.Gln508Ter
XM_024454181.1:c.172C>T	XP_024309949.1:p.Gln58Ter
XR_001741315.2:n.1714C>T