Canonical Allele Identifier: CA2654973908
Gene: COL6A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46125462_46125463insCA , CM000683.2:g.46125462_46125463insCA GRCh38
NC_000021.8:g.47545376_47545377insCA , CM000683.1:g.47545376_47545377insCA GRCh37
NC_000021.7:g.46369804_46369805insCA NCBI36
NG_008675.1:g.32344_32345insCA , LRG_476:g.32344_32345insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000397763.6:c.1817-3_1817-2insCA MANE Plus Clinical ENSP00000380870.1:n.1817-3_1817-2insCA
ENST00000300527.9:c.1817-3_1817-2insCA MANE Select ENSP00000300527.4:n.1817-3_1817-2insCA
ENST00000409416.6:c.1817-3_1817-2insCA ENSP00000387115.1:n.1817-3_1817-2insCA
ENST00000300527.8:c.1817-3_1817-2insCA ENSP00000300527.4:n.1817-3_1817-2insCA
ENST00000310645.9:c.1817-3_1817-2insCA ENSP00000312529.5:n.1817-3_1817-2insCA
ENST00000397763.5:c.1817-3_1817-2insCA ENSP00000380870.1:n.1817-3_1817-2insCA
ENST00000409416.5:c.1817-3_1817-2insCA ENSP00000387115.1:n.1817-3_1817-2insCA
ENST00000413758.1:c.485_486insCA ENSP00000395751.1:p.Asp163LysfsTer?
NM_001849.3:c.1817-3_1817-2insCA , LRG_476t1:c.1817-3_1817-2insCA NP_001840.3:n.1817-3_1817-2insCA
NM_058174.2:c.1817-3_1817-2insCA NP_478054.2:n.1817-3_1817-2insCA
NM_058175.2:c.1817-3_1817-2insCA NP_478055.2:n.1817-3_1817-2insCA
XM_011529451.1:c.1817-3_1817-2insCA XP_011527753.1:n.1817-3_1817-2insCA
XM_011529452.1:c.1817-3_1817-2insCA XP_011527754.1:n.1817-3_1817-2insCA
XR_937438.1:n.1894-3_1894-2insCA
XR_937439.1:n.1894-3_1894-2insCA
XR_937438.2:n.1901-3_1901-2insCA
XR_937439.2:n.1901-3_1901-2insCA
NM_001849.4:c.1817-3_1817-2insCA MANE Select NP_001840.3:n.1817-3_1817-2insCA
NM_058174.3:c.1817-3_1817-2insCA MANE Plus Clinical NP_478054.2:n.1817-3_1817-2insCA
NM_058175.3:c.1817-3_1817-2insCA NP_478055.2:n.1817-3_1817-2insCA