Canonical Allele Identifier: CA147300
Gene: COL6A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93794
ClinVar RCV Id: RCV000079731
dbSNP Id: rs1556425767

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45990464_45990465insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCGGGAGGACGGGGAGGGACGGGGAGG , CM000683.2:g.45990464_45990465insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCGGGAGGACGGGGAGGGACGGGGAGG GRCh38
NC_000021.8:g.47410378_47410379insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCGGGAGGACGGGGAGGGACGGGGAGG , CM000683.1:g.47410378_47410379insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCGGGAGGACGGGGAGGGACGGGGAGG GRCh37
NC_000021.7:g.46234806_46234807insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCGGGAGGACGGGGAGGGACGGGGAGG NCBI36
NG_008674.1:g.13716_13717insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCGGGAGGACGGGGAGGGACGGGGAGG , LRG_475:g.13716_13717insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCGGGAGGACGGGGAGGGACGGGGAGG

Transcript Alleles

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