Canonical Allele Identifier: CA2818100865
Gene: COL6A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46113608_46113609insCGCTGCCGAC , CM000683.2:g.46113608_46113609insCGCTGCCGAC GRCh38
NC_000021.8:g.47533522_47533523insCGCTGCCGAC , CM000683.1:g.47533522_47533523insCGCTGCCGAC GRCh37
NC_000021.7:g.46357950_46357951insCGCTGCCGAC NCBI36
NG_008675.1:g.20490_20491insCGCTGCCGAC , LRG_476:g.20490_20491insCGCTGCCGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000397763.6:c.736-400_736-399insCGCTGCCGAC MANE Plus Clinical ENSP00000380870.1:n.736-400_736-399insCGCTGCCGAC
ENST00000300527.9:c.736-400_736-399insCGCTGCCGAC MANE Select ENSP00000300527.4:n.736-400_736-399insCGCTGCCGAC
ENST00000409416.6:c.736-400_736-399insCGCTGCCGAC ENSP00000387115.1:n.736-400_736-399insCGCTGCCGAC
ENST00000300527.8:c.736-400_736-399insCGCTGCCGAC ENSP00000300527.4:n.736-400_736-399insCGCTGCCGAC
ENST00000310645.9:c.736-400_736-399insCGCTGCCGAC ENSP00000312529.5:n.736-400_736-399insCGCTGCCGAC
ENST00000397763.5:c.736-400_736-399insCGCTGCCGAC ENSP00000380870.1:n.736-400_736-399insCGCTGCCGAC
ENST00000409416.5:c.736-400_736-399insCGCTGCCGAC ENSP00000387115.1:n.736-400_736-399insCGCTGCCGAC
NM_001849.3:c.736-400_736-399insCGCTGCCGAC , LRG_476t1:c.736-400_736-399insCGCTGCCGAC NP_001840.3:n.736-400_736-399insCGCTGCCGAC
NM_058174.2:c.736-400_736-399insCGCTGCCGAC NP_478054.2:n.736-400_736-399insCGCTGCCGAC
NM_058175.2:c.736-400_736-399insCGCTGCCGAC NP_478055.2:n.736-400_736-399insCGCTGCCGAC
XM_011529451.1:c.736-400_736-399insCGCTGCCGAC XP_011527753.1:n.736-400_736-399insCGCTGCCGAC
XM_011529452.1:c.736-400_736-399insCGCTGCCGAC XP_011527754.1:n.736-400_736-399insCGCTGCCGAC
XR_937438.1:n.859-400_859-399insCGCTGCCGAC
XR_937439.1:n.859-400_859-399insCGCTGCCGAC
XR_937438.2:n.866-400_866-399insCGCTGCCGAC
XR_937439.2:n.866-400_866-399insCGCTGCCGAC
NM_001849.4:c.736-400_736-399insCGCTGCCGAC MANE Select NP_001840.3:n.736-400_736-399insCGCTGCCGAC
NM_058174.3:c.736-400_736-399insCGCTGCCGAC MANE Plus Clinical NP_478054.2:n.736-400_736-399insCGCTGCCGAC
NM_058175.3:c.736-400_736-399insCGCTGCCGAC NP_478055.2:n.736-400_736-399insCGCTGCCGAC