Canonical Allele Identifier: CA1022879740

Gene: COL6A1

Linked Data

• gnomAD v3: 21-45990442-A-ATGGACGGGGAGGGACGAGGAGGGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGG
• gnomAD v4: 21-45990442-A-ATGGACGGGGAGGGACGAGGAGGGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45990464_45990465insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG , CM000683.2:g.45990464_45990465insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG	GRCh38
NC_000021.8:g.47410378_47410379insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG , CM000683.1:g.47410378_47410379insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG	GRCh37
NC_000021.7:g.46234806_46234807insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG	NCBI36
NG_008674.1:g.13716_13717insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG , LRG_475:g.13716_13717insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361866.8:c.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG MANE Select	ENSP00000355180.3:n.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGT...
ENST00000361866.7:c.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG	ENSP00000355180.3:n.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGT...
ENST00000612273.1:c.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG	ENSP00000483630.1:n.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGT...
NM_001848.2:c.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG , LRG_475t1:c.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG	NP_001839.2:n.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGTGACCGG...
NM_001848.3:c.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGTGACCGGGGAGGGATGGGGTGGACGGGGAGGGACGAGGAGG MANE Select	NP_001839.2:n.1002+42_1002+43insGATGGGGTGGACAGCGTGAAGGTGACCGG...