Canonical Allele Identifier: CA6958270
Gene: COG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39660815T>C , CM000675.2:g.39660815T>C GRCh38
NC_000013.10:g.40234952T>C , CM000675.1:g.40234952T>C GRCh37
NC_000013.9:g.39132952T>C NCBI36
NG_028352.1:g.10189T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000455146.8:c.303T>C MANE Select ENSP00000397441.2:p.Leu101=
ENST00000356576.8:c.*140T>C ENSP00000348983.4:n.*140T>C
ENST00000416691.5:c.303T>C ENSP00000403733.1:p.Leu101=
ENST00000422759.6:n.368T>C
ENST00000455146.7:c.303T>C ENSP00000397441.2:p.Leu101=
ENST00000536488.5:c.118T>C
ENST00000543804.5:c.*64T>C ENSP00000440473.1:n.*64T>C
NM_001145079.1:c.303T>C NP_001138551.1:p.Leu101=
NM_020751.2:c.303T>C NP_065802.1:p.Leu101=
NR_026745.1:n.468T>C
XM_011535168.1:c.303T>C XP_011533470.1:p.Leu101=
XM_011535169.1:c.147T>C XP_011533471.1:p.Leu49=
XM_011535170.1:c.147T>C XP_011533472.1:p.Leu49=
NM_020751.3:c.303T>C MANE Select NP_065802.1:p.Leu101=
NM_001145079.2:c.303T>C NP_001138551.1:p.Leu101=