Canonical Allele Identifier: CA2118745107
Gene: COL4A1 HGNC NCBI

Linked Data

dbSNP Id: rs1878669252

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110192297_110192300del , CM000675.2:g.110192297_110192300del GRCh38
NC_000013.10:g.110844644_110844647del , CM000675.1:g.110844644_110844647del GRCh37
NC_000013.9:g.109642645_109642648del NCBI36
NG_011544.2:g.119855_119858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375820.10:c.1466-11_1466-8del MANE Select ENSP00000364979.4:n.1466-11_1466-8del
ENST00000543140.6:c.1466-11_1466-8del ENSP00000443348.1:n.1466-11_1466-8del
ENST00000649738.1:n.1596-11_1596-8del
ENST00000375820.8:c.1466-11_1466-8del ENSP00000364979.4:n.1466-11_1466-8del
ENST00000543140.5:c.1466-11_1466-8del ENSP00000443348.1:n.1466-11_1466-8del
NM_001303110.1:c.1466-11_1466-8del NP_001290039.1:n.1466-11_1466-8del
NM_001845.5:c.1466-11_1466-8del NP_001836.3:n.1466-11_1466-8del
XM_011521048.1:c.1274-11_1274-8del XP_011519350.1:n.1274-11_1274-8del
XM_011521048.2:c.1274-11_1274-8del XP_011519350.1:n.1274-11_1274-8del
NM_001845.6:c.1466-11_1466-8del MANE Select NP_001836.3:n.1466-11_1466-8del
NM_001303110.2:c.1466-11_1466-8del NP_001290039.1:n.1466-11_1466-8del