Canonical Allele Identifier: CA2118745159
Gene: COL4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110192425A= , CM000675.2:g.110192425A= GRCh38
NC_000013.10:g.110844772A= , CM000675.1:g.110844772A= GRCh37
NC_000013.9:g.109642773A= NCBI36
NG_011544.2:g.119725T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375820.10:c.1466-141T= MANE Select ENSP00000364979.4:n.1466-141T=
ENST00000543140.6:c.1466-141T= ENSP00000443348.1:n.1466-141T=
ENST00000649738.1:n.1596-141T=
ENST00000375820.8:c.1466-141T= ENSP00000364979.4:n.1466-141T=
ENST00000543140.5:c.1466-141T= ENSP00000443348.1:n.1466-141T=
NM_001303110.1:c.1466-141T= NP_001290039.1:n.1466-141T=
NM_001845.5:c.1466-141T= NP_001836.3:n.1466-141T=
XM_011521048.1:c.1274-141T= XP_011519350.1:n.1274-141T=
XM_011521048.2:c.1274-141T= XP_011519350.1:n.1274-141T=
NM_001845.6:c.1466-141T= MANE Select NP_001836.3:n.1466-141T=
NM_001303110.2:c.1466-141T= NP_001290039.1:n.1466-141T=