Canonical Allele Identifier: CA2818093004
Gene: COL6A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45990465_45990466insCGGGGAGGGCTGGGGTGGACAGTGTGAAGGTGACCCGGGGACGGACGGGGAGGGACGGGGAGGG , CM000683.2:g.45990465_45990466insCGGGGAGGGCTGGGGTGGACAGTGTGAAGGTGACCCGGGGACGGACGGGGAGGGACGGGGAGGG GRCh38
NC_000021.8:g.47410379_47410380insCGGGGAGGGCTGGGGTGGACAGTGTGAAGGTGACCCGGGGACGGACGGGGAGGGACGGGGAGGG , CM000683.1:g.47410379_47410380insCGGGGAGGGCTGGGGTGGACAGTGTGAAGGTGACCCGGGGACGGACGGGGAGGGACGGGGAGGG GRCh37
NC_000021.7:g.46234807_46234808insCGGGGAGGGCTGGGGTGGACAGTGTGAAGGTGACCCGGGGACGGACGGGGAGGGACGGGGAGGG NCBI36
NG_008674.1:g.13717_13718insCGGGGAGGGCTGGGGTGGACAGTGTGAAGGTGACCCGGGGACGGACGGGGAGGGACGGGGAGGG , LRG_475:g.13717_13718insCGGGGAGGGCTGGGGTGGACAGTGTGAAGGTGACCCGGGGACGGACGGGGAGGGACGGGGAGGG

Transcript Alleles

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