Canonical Allele Identifier: CA638178896

Gene: COL6A1

Linked Data

• ClinVar Variation Id: 1366244
• ClinVar RCV Id: RCV001944581
• dbSNP Id: rs1569518218
• gnomAD v2: 21-47410353-A-AGGATGGACGGGGAGGGACGAGGAGGGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGG
• gnomAD v3: 21-45990439-A-AGGATGGACGGGGAGGGACGAGGAGGGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGG
• gnomAD v4: 21-45990439-A-AGGATGGACGGGGAGGGACGAGGAGGGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGG
• MyVariant Identifiers: chr21:g.47410353_47410354insGGATGGACGGGGAGGGACGAGGAGGGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGG (hg19) ; chr21:g.45990439_45990440insGGATGGACGGGGAGGGACGAGGAGGGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45990464_45990465insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGATGGACGGGGAGGGACGAGGAGG , CM000683.2:g.45990464_45990465insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGATGGACGGGGAGGGACGAGGAGG	GRCh38
NC_000021.8:g.47410378_47410379insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGATGGACGGGGAGGGACGAGGAGG , CM000683.1:g.47410378_47410379insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGATGGACGGGGAGGGACGAGGAGG	GRCh37
NC_000021.7:g.46234806_46234807insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGATGGACGGGGAGGGACGAGGAGG	NCBI36
NG_008674.1:g.13716_13717insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGATGGACGGGGAGGGACGAGGAGG , LRG_475:g.13716_13717insGACGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGATGGACGGGGAGGGACGAGGAGG

Transcript Alleles

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