Canonical Allele Identifier: CA2392434203
Gene: COL6A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45990467_45990512delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC , CM000683.2:g.45990467_45990512delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC GRCh38
NC_000021.8:g.47410381_47410426delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC , CM000683.1:g.47410381_47410426delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC GRCh37
NC_000021.7:g.46234809_46234854delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC NCBI36
NG_008674.1:g.13719_13764delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC , LRG_475:g.13719_13764delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000361866.8:c.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC MANE Select ENSP00000355180.3:n.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGA...
ENST00000361866.7:c.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC ENSP00000355180.3:n.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGA...
ENST00000612273.1:c.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC ENSP00000483630.1:n.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGA...
NM_001848.2:c.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC , LRG_475t1:c.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC NP_001839.2:n.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGACGGAGT...
NM_001848.3:c.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGACGGAGTGGACGGCGTGAAGGTGACCC MANE Select NP_001839.2:n.1002+45_1002+90delinsTGGGGCGAGATGGGGAGGGACGGAGT...