Canonical Allele Identifier: CA2654972679
Gene: COL6A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45990581_45990582insCGAGATGGGGAGGGATGGGG , CM000683.2:g.45990581_45990582insCGAGATGGGGAGGGATGGGG GRCh38
NC_000021.8:g.47410495_47410496insCGAGATGGGGAGGGATGGGG , CM000683.1:g.47410495_47410496insCGAGATGGGGAGGGATGGGG GRCh37
NC_000021.7:g.46234923_46234924insCGAGATGGGGAGGGATGGGG NCBI36
NG_008674.1:g.13833_13834insCGAGATGGGGAGGGATGGGG , LRG_475:g.13833_13834insCGAGATGGGGAGGGATGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361866.8:c.1002+159_1002+160insCGAGATGGGGAGGGATGGGG MANE Select ENSP00000355180.3:n.1002+159_1002+160insCGAGATGGGGAGGGATGGGG
ENST00000361866.7:c.1002+159_1002+160insCGAGATGGGGAGGGATGGGG ENSP00000355180.3:n.1002+159_1002+160insCGAGATGGGGAGGGATGGGG
ENST00000612273.1:c.1002+159_1002+160insCGAGATGGGGAGGGATGGGG ENSP00000483630.1:n.1002+159_1002+160insCGAGATGGGGAGGGATGGGG
NM_001848.2:c.1002+159_1002+160insCGAGATGGGGAGGGATGGGG , LRG_475t1:c.1002+159_1002+160insCGAGATGGGGAGGGATGGGG NP_001839.2:n.1002+159_1002+160insCGAGATGGGGAGGGATGGGG
NM_001848.3:c.1002+159_1002+160insCGAGATGGGGAGGGATGGGG MANE Select NP_001839.2:n.1002+159_1002+160insCGAGATGGGGAGGGATGGGG