Canonical Allele Identifier: CA2694428791
Gene: COL4A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108156966_108156975del , CM000685.2:g.108156966_108156975del GRCh38
NC_000023.10:g.107400196_107400205del , CM000685.1:g.107400196_107400205del GRCh37
NC_000023.9:g.107286852_107286861del NCBI36
NG_012059.2:g.287505_287514del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334504.12:c.*30_*39del MANE Select ENSP00000334733.7:n.*30_*39del
ENST00000334504.11:c.*30_*39del ENSP00000334733.7:n.*30_*39del
ENST00000372216.8:c.*30_*39del ENSP00000361290.4:n.*30_*39del
ENST00000394872.6:c.*30_*39del ENSP00000378340.3:n.*30_*39del
ENST00000538570.5:c.*30_*39del ENSP00000445236.1:n.*30_*39del
ENST00000545689.2:c.*30_*39del ENSP00000443707.2:n.*30_*39del
ENST00000621266.4:c.*30_*39del ENSP00000482970.1:n.*30_*39del
NM_001287758.1:c.*30_*39del NP_001274687.1:n.*30_*39del
NM_001287759.1:c.*30_*39del NP_001274688.1:n.*30_*39del
NM_001287760.1:c.*30_*39del NP_001274689.1:n.*30_*39del
NM_001847.3:c.*30_*39del NP_001838.2:n.*30_*39del
NM_033641.3:c.*30_*39del NP_378667.1:n.*30_*39del
XM_006724617.2:c.*30_*39del XP_006724680.1:n.*30_*39del
XM_011530852.1:c.*30_*39del XP_011529154.1:n.*30_*39del
XM_011530853.1:c.*30_*39del XP_011529155.1:n.*30_*39del
XM_006724617.3:c.*30_*39del XP_006724680.1:n.*30_*39del
XM_011530852.2:c.*30_*39del XP_011529154.1:n.*30_*39del
XM_011530853.3:c.*30_*39del XP_011529155.1:n.*30_*39del
NM_001847.4:c.*30_*39del NP_001838.2:n.*30_*39del
NM_033641.4:c.*30_*39del MANE Select NP_378667.1:n.*30_*39del
NM_001287758.2:c.*30_*39del NP_001274687.1:n.*30_*39del
NM_001287759.2:c.*30_*39del NP_001274688.1:n.*30_*39del
NM_001287760.2:c.*30_*39del NP_001274689.1:n.*30_*39del