Canonical Allele Identifier: CA2392507297

Gene: COL6A2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46125428_46125438delinsTCCCCGGTACC , CM000683.2:g.46125428_46125438delinsTCCCCGGTACC	GRCh38
NC_000021.8:g.47545342_47545352delinsTCCCCGGTACC , CM000683.1:g.47545342_47545352delinsTCCCCGGTACC	GRCh37
NC_000021.7:g.46369770_46369780delinsTCCCCGGTACC	NCBI36
NG_008675.1:g.32310_32320delinsTCCCCGGTACC , LRG_476:g.32310_32320delinsTCCCCGGTACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.1817-37_1817-27delinsTCCCCGGTACC MANE Plus Clinical	ENSP00000380870.1:n.1817-37_1817-27delinsTCCCCGGTACC
ENST00000300527.9:c.1817-37_1817-27delinsTCCCCGGTACC MANE Select	ENSP00000300527.4:n.1817-37_1817-27delinsTCCCCGGTACC
ENST00000409416.6:c.1817-37_1817-27delinsTCCCCGGTACC	ENSP00000387115.1:n.1817-37_1817-27delinsTCCCCGGTACC
ENST00000300527.8:c.1817-37_1817-27delinsTCCCCGGTACC	ENSP00000300527.4:n.1817-37_1817-27delinsTCCCCGGTACC
ENST00000310645.9:c.1817-37_1817-27delinsTCCCCGGTACC	ENSP00000312529.5:n.1817-37_1817-27delinsTCCCCGGTACC
ENST00000397763.5:c.1817-37_1817-27delinsTCCCCGGTACC	ENSP00000380870.1:n.1817-37_1817-27delinsTCCCCGGTACC
ENST00000409416.5:c.1817-37_1817-27delinsTCCCCGGTACC	ENSP00000387115.1:n.1817-37_1817-27delinsTCCCCGGTACC
ENST00000413758.1:c.451_461delinsTCCCCGGTACC	ENSP00000395751.1:p.Ser151=
NM_001849.3:c.1817-37_1817-27delinsTCCCCGGTACC , LRG_476t1:c.1817-37_1817-27delinsTCCCCGGTACC	NP_001840.3:n.1817-37_1817-27delinsTCCCCGGTACC
NM_058174.2:c.1817-37_1817-27delinsTCCCCGGTACC	NP_478054.2:n.1817-37_1817-27delinsTCCCCGGTACC
NM_058175.2:c.1817-37_1817-27delinsTCCCCGGTACC	NP_478055.2:n.1817-37_1817-27delinsTCCCCGGTACC
XM_011529451.1:c.1817-37_1817-27delinsTCCCCGGTACC	XP_011527753.1:n.1817-37_1817-27delinsTCCCCGGTACC
XM_011529452.1:c.1817-37_1817-27delinsTCCCCGGTACC	XP_011527754.1:n.1817-37_1817-27delinsTCCCCGGTACC
XR_937438.1:n.1894-37_1894-27delinsTCCCCGGTACC
XR_937439.1:n.1894-37_1894-27delinsTCCCCGGTACC
XR_937438.2:n.1901-37_1901-27delinsTCCCCGGTACC
XR_937439.2:n.1901-37_1901-27delinsTCCCCGGTACC
NM_001849.4:c.1817-37_1817-27delinsTCCCCGGTACC MANE Select	NP_001840.3:n.1817-37_1817-27delinsTCCCCGGTACC
NM_058174.3:c.1817-37_1817-27delinsTCCCCGGTACC MANE Plus Clinical	NP_478054.2:n.1817-37_1817-27delinsTCCCCGGTACC
NM_058175.3:c.1817-37_1817-27delinsTCCCCGGTACC	NP_478055.2:n.1817-37_1817-27delinsTCCCCGGTACC