Canonical Allele Identifier: CA673644183

Gene: OPCML

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.132959967A>T , CM000673.2:g.132959967A>T	GRCh38
NC_000011.9:g.132829862A>T , CM000673.1:g.132829862A>T	GRCh37
NC_000011.8:g.132335072A>T	NCBI36
NG_012107.1:g.577542T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524381.6:c.62-16957T>A MANE Select	ENSP00000434750.1:n.62-16957T>A
ENST00000524381.5:c.62-16957T>A	ENSP00000434750.1:n.62-16957T>A
ENST00000529038.5:n.140-302648T>A
NM_001012393.1:c.62-16957T>A	NP_001012393.1:n.62-16957T>A
XM_006718846.1:c.62-16957T>A	XP_006718909.1:n.62-16957T>A
XM_011542856.1:c.-41-16957T>A	XP_011541158.1:n.-41-16957T>A
XR_948205.1:n.33A>T
NM_001012393.2:c.62-16957T>A	NP_001012393.1:n.62-16957T>A
NM_001319104.1:c.-133-302648T>A	NP_001306033.1:n.-133-302648T>A
XM_006718846.3:c.62-16957T>A	XP_006718909.1:n.62-16957T>A
XM_011542856.3:c.-41-16957T>A	XP_011541158.1:n.-41-16957T>A
XR_948205.2:n.21A>T
NM_001012393.3:c.62-16957T>A	NP_001012393.1:n.62-16957T>A
NM_001319104.2:c.-133-302648T>A	NP_001306033.1:n.-133-302648T>A
NM_001012393.5:c.62-16957T>A MANE Select	NP_001012393.1:n.62-16957T>A
NM_001319104.4:c.-133-302648T>A	NP_001306033.1:n.-133-302648T>A