Canonical Allele Identifier: CA2654973906

Gene: COL6A2

Linked Data

• gnomAD v4: 21-46125454-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46125454_46125455insT , CM000683.2:g.46125454_46125455insT	GRCh38
NC_000021.8:g.47545368_47545369insT , CM000683.1:g.47545368_47545369insT	GRCh37
NC_000021.7:g.46369796_46369797insT	NCBI36
NG_008675.1:g.32336_32337insT , LRG_476:g.32336_32337insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.1817-11_1817-10insT MANE Plus Clinical	ENSP00000380870.1:n.1817-11_1817-10insT
ENST00000300527.9:c.1817-11_1817-10insT MANE Select	ENSP00000300527.4:n.1817-11_1817-10insT
ENST00000409416.6:c.1817-11_1817-10insT	ENSP00000387115.1:n.1817-11_1817-10insT
ENST00000300527.8:c.1817-11_1817-10insT	ENSP00000300527.4:n.1817-11_1817-10insT
ENST00000310645.9:c.1817-11_1817-10insT	ENSP00000312529.5:n.1817-11_1817-10insT
ENST00000397763.5:c.1817-11_1817-10insT	ENSP00000380870.1:n.1817-11_1817-10insT
ENST00000409416.5:c.1817-11_1817-10insT	ENSP00000387115.1:n.1817-11_1817-10insT
ENST00000413758.1:c.477_478insT	ENSP00000395751.1:p.Thr160TyrfsTer6
NM_001849.3:c.1817-11_1817-10insT , LRG_476t1:c.1817-11_1817-10insT	NP_001840.3:n.1817-11_1817-10insT
NM_058174.2:c.1817-11_1817-10insT	NP_478054.2:n.1817-11_1817-10insT
NM_058175.2:c.1817-11_1817-10insT	NP_478055.2:n.1817-11_1817-10insT
XM_011529451.1:c.1817-11_1817-10insT	XP_011527753.1:n.1817-11_1817-10insT
XM_011529452.1:c.1817-11_1817-10insT	XP_011527754.1:n.1817-11_1817-10insT
XR_937438.1:n.1894-11_1894-10insT
XR_937439.1:n.1894-11_1894-10insT
XR_937438.2:n.1901-11_1901-10insT
XR_937439.2:n.1901-11_1901-10insT
NM_001849.4:c.1817-11_1817-10insT MANE Select	NP_001840.3:n.1817-11_1817-10insT
NM_058174.3:c.1817-11_1817-10insT MANE Plus Clinical	NP_478054.2:n.1817-11_1817-10insT
NM_058175.3:c.1817-11_1817-10insT	NP_478055.2:n.1817-11_1817-10insT