Canonical Allele Identifier: CA6958488

Gene: COG6

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.39687729T>C , CM000675.2:g.39687729T>C	GRCh38
NC_000013.10:g.40261866T>C , CM000675.1:g.40261866T>C	GRCh37
NC_000013.9:g.39159866T>C	NCBI36
NG_028352.1:g.37103T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455146.8:c.939T>C MANE Select	ENSP00000397441.2:p.Ala313=
ENST00000356576.8:c.*776T>C	ENSP00000348983.4:n.*776T>C
ENST00000416691.5:c.939T>C	ENSP00000403733.1:p.Ala313=
ENST00000455146.7:c.939T>C	ENSP00000397441.2:p.Ala313=
ENST00000460701.1:n.187T>C
NM_001145079.1:c.939T>C	NP_001138551.1:p.Ala313=
NM_020751.2:c.939T>C	NP_065802.1:p.Ala313=
NR_026745.1:n.1104T>C
XM_011535168.1:c.939T>C	XP_011533470.1:p.Ala313=
XM_011535169.1:c.783T>C	XP_011533471.1:p.Ala261=
XM_011535170.1:c.783T>C	XP_011533472.1:p.Ala261=
NM_020751.3:c.939T>C MANE Select	NP_065802.1:p.Ala313=
NM_001145079.2:c.939T>C	NP_001138551.1:p.Ala313=