Canonical Allele Identifier: CA2392507333
Gene: COL6A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46125461_46125463delinsCCA , CM000683.2:g.46125461_46125463delinsCCA GRCh38
NC_000021.8:g.47545375_47545377delinsCCA , CM000683.1:g.47545375_47545377delinsCCA GRCh37
NC_000021.7:g.46369803_46369805delinsCCA NCBI36
NG_008675.1:g.32343_32345delinsCCA , LRG_476:g.32343_32345delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000397763.6:c.1817-4_1817-2delinsCCA MANE Plus Clinical ENSP00000380870.1:n.1817-4_1817-2delinsCCA
ENST00000300527.9:c.1817-4_1817-2delinsCCA MANE Select ENSP00000300527.4:n.1817-4_1817-2delinsCCA
ENST00000409416.6:c.1817-4_1817-2delinsCCA ENSP00000387115.1:n.1817-4_1817-2delinsCCA
ENST00000300527.8:c.1817-4_1817-2delinsCCA ENSP00000300527.4:n.1817-4_1817-2delinsCCA
ENST00000310645.9:c.1817-4_1817-2delinsCCA ENSP00000312529.5:n.1817-4_1817-2delinsCCA
ENST00000397763.5:c.1817-4_1817-2delinsCCA ENSP00000380870.1:n.1817-4_1817-2delinsCCA
ENST00000409416.5:c.1817-4_1817-2delinsCCA ENSP00000387115.1:n.1817-4_1817-2delinsCCA
ENST00000413758.1:c.484_486delinsCCA ENSP00000395751.1:p.Pro162=
NM_001849.3:c.1817-4_1817-2delinsCCA , LRG_476t1:c.1817-4_1817-2delinsCCA NP_001840.3:n.1817-4_1817-2delinsCCA
NM_058174.2:c.1817-4_1817-2delinsCCA NP_478054.2:n.1817-4_1817-2delinsCCA
NM_058175.2:c.1817-4_1817-2delinsCCA NP_478055.2:n.1817-4_1817-2delinsCCA
XM_011529451.1:c.1817-4_1817-2delinsCCA XP_011527753.1:n.1817-4_1817-2delinsCCA
XM_011529452.1:c.1817-4_1817-2delinsCCA XP_011527754.1:n.1817-4_1817-2delinsCCA
XR_937438.1:n.1894-4_1894-2delinsCCA
XR_937439.1:n.1894-4_1894-2delinsCCA
XR_937438.2:n.1901-4_1901-2delinsCCA
XR_937439.2:n.1901-4_1901-2delinsCCA
NM_001849.4:c.1817-4_1817-2delinsCCA MANE Select NP_001840.3:n.1817-4_1817-2delinsCCA
NM_058174.3:c.1817-4_1817-2delinsCCA MANE Plus Clinical NP_478054.2:n.1817-4_1817-2delinsCCA
NM_058175.3:c.1817-4_1817-2delinsCCA NP_478055.2:n.1817-4_1817-2delinsCCA