Canonical Allele Identifier: CA2392434181
Gene: COL6A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45990459_45990479delinsAGGAGGAATGGGGCGAGATGG , CM000683.2:g.45990459_45990479delinsAGGAGGAATGGGGCGAGATGG GRCh38
NC_000021.8:g.47410373_47410393delinsAGGAGGAATGGGGCGAGATGG , CM000683.1:g.47410373_47410393delinsAGGAGGAATGGGGCGAGATGG GRCh37
NC_000021.7:g.46234801_46234821delinsAGGAGGAATGGGGCGAGATGG NCBI36
NG_008674.1:g.13711_13731delinsAGGAGGAATGGGGCGAGATGG , LRG_475:g.13711_13731delinsAGGAGGAATGGGGCGAGATGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361866.8:c.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATGG MANE Select ENSP00000355180.3:n.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATG...
ENST00000361866.7:c.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATGG ENSP00000355180.3:n.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATG...
ENST00000612273.1:c.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATGG ENSP00000483630.1:n.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATG...
NM_001848.2:c.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATGG , LRG_475t1:c.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATGG NP_001839.2:n.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATGG
NM_001848.3:c.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATGG MANE Select NP_001839.2:n.1002+37_1002+57delinsAGGAGGAATGGGGCGAGATGG