Canonical Allele Identifier: CA2654970972
Gene: COL6A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45990465_45990466insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG , CM000683.2:g.45990465_45990466insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG GRCh38
NC_000021.8:g.47410379_47410380insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG , CM000683.1:g.47410379_47410380insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG GRCh37
NC_000021.7:g.46234807_46234808insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG NCBI36
NG_008674.1:g.13717_13718insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG , LRG_475:g.13717_13718insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361866.8:c.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG MANE Select ENSP00000355180.3:n.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGA...
ENST00000361866.7:c.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG ENSP00000355180.3:n.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGA...
ENST00000612273.1:c.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG ENSP00000483630.1:n.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGA...
NM_001848.2:c.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG , LRG_475t1:c.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG NP_001839.2:n.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGAGTGAAG...
NM_001848.3:c.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGAGTGAAGGAGACCAGGGGAGGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG MANE Select NP_001839.2:n.1002+43_1002+44insCGGGGAGGGATGGGGTGGACAGAGTGAAG...