Canonical Allele Identifier: CA1022880442
Gene: COL6A1 HGNC NCBI

Linked Data

dbSNP Id: rs2077769094

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45990465_45990466insCGGGGAGGGATGGGGTGGACAGCGTGAAGGTGACCAGGGGAAGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG , CM000683.2:g.45990465_45990466insCGGGGAGGGATGGGGTGGACAGCGTGAAGGTGACCAGGGGAAGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG GRCh38
NC_000021.8:g.47410379_47410380insCGGGGAGGGATGGGGTGGACAGCGTGAAGGTGACCAGGGGAAGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG , CM000683.1:g.47410379_47410380insCGGGGAGGGATGGGGTGGACAGCGTGAAGGTGACCAGGGGAAGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG GRCh37
NC_000021.7:g.46234807_46234808insCGGGGAGGGATGGGGTGGACAGCGTGAAGGTGACCAGGGGAAGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG NCBI36
NG_008674.1:g.13717_13718insCGGGGAGGGATGGGGTGGACAGCGTGAAGGTGACCAGGGGAAGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG , LRG_475:g.13717_13718insCGGGGAGGGATGGGGTGGACAGCGTGAAGGTGACCAGGGGAAGGATGGGGTGGACAGTGTGAAGGTGACCAGGGGAAGGACGGGGAGGGACGGGGAGGG

Transcript Alleles

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