Canonical Allele Identifier: CA2166365217

Gene: OCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27926528_27926529delinsAG , CM000677.2:g.27926528_27926529delinsAG	GRCh38
NC_000015.9:g.28171674_28171675delinsAG , CM000677.1:g.28171674_28171675delinsAG	GRCh37
NC_000015.8:g.25845269_25845270delinsAG	NCBI36
NG_009846.1:g.177784_177785delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354638.8:c.1952-275_1952-274delinsCT MANE Select	ENSP00000346659.3:n.1952-275_1952-274delinsCT
ENST00000353809.9:c.1880-275_1880-274delinsCT	ENSP00000261276.8:n.1880-275_1880-274delinsCT
ENST00000354638.7:c.1952-275_1952-274delinsCT	ENSP00000346659.3:n.1952-275_1952-274delinsCT
NM_000275.2:c.1952-275_1952-274delinsCT	NP_000266.2:n.1952-275_1952-274delinsCT
NM_001300984.1:c.1880-275_1880-274delinsCT	NP_001287913.1:n.1880-275_1880-274delinsCT
XM_011521639.1:c.1976-275_1976-274delinsCT	XP_011519941.1:n.1976-275_1976-274delinsCT
XM_011521640.1:c.1952-275_1952-274delinsCT	XP_011519942.1:n.1952-275_1952-274delinsCT
XM_011521641.1:c.1976-275_1976-274delinsCT	XP_011519943.1:n.1976-275_1976-274delinsCT
XM_011521642.1:c.1904-275_1904-274delinsCT	XP_011519944.1:n.1904-275_1904-274delinsCT
XM_011521643.1:c.1904-275_1904-274delinsCT	XP_011519945.1:n.1904-275_1904-274delinsCT
XM_011521644.1:c.1838-275_1838-274delinsCT	XP_011519946.1:n.1838-275_1838-274delinsCT
XM_011521645.1:c.1976-275_1976-274delinsCT	XP_011519947.1:n.1976-275_1976-274delinsCT
XM_011521640.2:c.1952-275_1952-274delinsCT	XP_011519942.1:n.1952-275_1952-274delinsCT
XM_017022255.1:c.1976-275_1976-274delinsCT	XP_016877744.1:n.1976-275_1976-274delinsCT
XM_017022256.1:c.1976-275_1976-274delinsCT	XP_016877745.1:n.1976-275_1976-274delinsCT
XM_017022257.1:c.1904-275_1904-274delinsCT	XP_016877746.1:n.1904-275_1904-274delinsCT
XM_017022258.1:c.1976-275_1976-274delinsCT	XP_016877747.1:n.1976-275_1976-274delinsCT
XM_017022259.1:c.1904-275_1904-274delinsCT	XP_016877748.1:n.1904-275_1904-274delinsCT
XM_017022260.1:c.1838-275_1838-274delinsCT	XP_016877749.1:n.1838-275_1838-274delinsCT
XM_017022261.1:c.1781-275_1781-274delinsCT	XP_016877750.1:n.1781-275_1781-274delinsCT
XM_017022262.1:c.1976-275_1976-274delinsCT	XP_016877751.1:n.1976-275_1976-274delinsCT
XM_017022263.1:c.1976-275_1976-274delinsCT	XP_016877752.1:n.1976-275_1976-274delinsCT
XM_017022264.1:c.1976-275_1976-274delinsCT	XP_016877753.1:n.1976-275_1976-274delinsCT
NM_000275.3:c.1952-275_1952-274delinsCT MANE Select	NP_000266.2:n.1952-275_1952-274delinsCT
NM_001300984.2:c.1880-275_1880-274delinsCT	NP_001287913.1:n.1880-275_1880-274delinsCT