Canonical Allele Identifier: CA496228640

Gene: COG4

Linked Data

• MyVariant Identifiers: chr16:g.70517761A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483858A>G , CM000678.2:g.70483858A>G	GRCh38
NC_000016.9:g.70517761A>G , CM000678.1:g.70517761A>G	GRCh37
NC_000016.8:g.69075262A>G	NCBI36
NG_027529.1:g.44697T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1898T>C	ENSP00000461912.2:n.*1898T>C
ENST00000703106.1:c.1867T>C	ENSP00000515173.1:n.1867T>C
ENST00000703107.1:c.*1751T>C	ENSP00000515174.1:n.*1751T>C
ENST00000703108.1:c.*270T>C	ENSP00000515175.1:n.*270T>C
ENST00000703109.1:c.1855T>C	ENSP00000515176.1:p.Leu619=
ENST00000703110.1:c.*1324T>C	ENSP00000515177.1:n.*1324T>C
ENST00000703111.1:n.1829T>C
ENST00000703112.1:n.2595T>C
ENST00000703113.1:c.*1235T>C	ENSP00000515178.1:n.*1235T>C
ENST00000703114.1:c.*471T>C	ENSP00000515179.1:n.*471T>C
ENST00000703115.1:c.935T>C	ENSP00000515180.1:n.935T>C
ENST00000323786.10:c.1822T>C MANE Select	ENSP00000315775.5:p.Leu608=
ENST00000564415.6:c.*1602T>C	ENSP00000456653.2:n.*1602T>C
ENST00000674443.1:c.1747T>C	ENSP00000501405.1:p.Leu583=
ENST00000323786.9:c.1822T>C	ENSP00000315775.5:p.Leu608=
ENST00000393612.8:c.1759T>C	ENSP00000377236.5:p.Leu587=
ENST00000482252.5:c.1969T>C	ENSP00000432802.1:n.1969T>C
ENST00000526700.5:n.998T>C
ENST00000530314.5:n.2501T>C
ENST00000564315.1:n.282T>C
ENST00000564415.5:c.*1602T>C	ENSP00000456653.1:n.*1602T>C
NM_001195139.1:c.1759T>C	NP_001182068.1:p.Leu587=
NM_015386.2:c.1822T>C	NP_056201.2:p.Leu608=
XM_011522981.1:c.1396T>C	XP_011521283.1:p.Leu466=
XR_933266.1:n.1768T>C
XR_933267.1:n.1768T>C
XM_011522981.3:c.1396T>C	XP_011521283.1:p.Leu466=
XM_024450224.1:c.841T>C	XP_024305992.1:p.Leu281=
XR_001751889.1:n.1705T>C
XR_933266.2:n.1768T>C
NM_015386.3:c.1822T>C MANE Select	NP_056201.2:p.Leu608=
NM_001195139.2:c.1747T>C	NP_001182068.2:p.Leu583=
NM_001365426.1:c.1396T>C	NP_001352355.1:p.Leu466=
NR_158212.1:n.1781T>C