Canonical Allele Identifier: CA560465773

Gene: POC5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75692544A>T , CM000667.2:g.75692544A>T	GRCh38
NC_000005.9:g.74988369A>T , CM000667.1:g.74988369A>T	GRCh37
NC_000005.8:g.75024125A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428202.7:c.691-44T>A MANE Select	ENSP00000410216.2:n.691-44T>A
ENST00000357564.4:n.245-44T>A
ENST00000428202.6:c.691-44T>A	ENSP00000410216.2:n.691-44T>A
ENST00000446329.6:c.616-44T>A	ENSP00000399481.2:n.616-44T>A
ENST00000503835.5:c.340-44T>A	ENSP00000424264.1:n.340-44T>A
ENST00000510798.5:c.340-44T>A	ENSP00000426796.1:n.340-44T>A
ENST00000514838.6:c.607-44T>A	ENSP00000420971.1:n.607-44T>A
NM_001099271.1:c.691-44T>A	NP_001092741.1:n.691-44T>A
NM_152408.2:c.616-44T>A	NP_689621.2:n.616-44T>A
XM_005248436.1:c.691-44T>A	XP_005248493.1:n.691-44T>A
XM_005248437.3:c.691-44T>A	XP_005248494.2:n.691-44T>A
XM_011543158.1:c.691-44T>A	XP_011541460.1:n.691-44T>A
XM_011543159.1:c.340-44T>A	XP_011541461.1:n.340-44T>A
XM_011543160.1:c.340-44T>A	XP_011541462.1:n.340-44T>A
XM_011543158.2:c.691-44T>A	XP_011541460.1:n.691-44T>A
XM_017009037.2:c.691-1982T>A	XP_016864526.1:n.691-1982T>A
XM_017009040.2:c.340-1982T>A	XP_016864529.1:n.340-1982T>A
XM_024454362.1:c.691-44T>A	XP_024310130.1:n.691-44T>A
XM_024454363.1:c.340-44T>A	XP_024310131.1:n.340-44T>A
XR_001741999.1:n.888-44T>A
NM_001099271.2:c.691-44T>A MANE Select	NP_001092741.1:n.691-44T>A
NM_152408.3:c.616-44T>A	NP_689621.2:n.616-44T>A