Canonical Allele Identifier: CA2118732259
Gene: COL4A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110169218C= , CM000675.2:g.110169218C= GRCh38
NC_000013.10:g.110821565C= , CM000675.1:g.110821565C= GRCh37
NC_000013.9:g.109619566C= NCBI36
NG_011544.2:g.142932G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375820.10:c.3876+411G= MANE Select ENSP00000364979.4:n.3876+411G=
ENST00000650424.1:c.32+411G=
ENST00000375820.8:c.3876+411G= ENSP00000364979.4:n.3876+411G=
NM_001845.5:c.3876+411G= NP_001836.3:n.3876+411G=
XM_011521048.1:c.3684+411G= XP_011519350.1:n.3684+411G=
XM_011521048.2:c.3684+411G= XP_011519350.1:n.3684+411G=
NM_001845.6:c.3876+411G= MANE Select NP_001836.3:n.3876+411G=
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