Canonical Allele Identifier: CA2450634622
Gene: COL4A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108440048C= , CM000685.2:g.108440048C= GRCh38
NC_000023.10:g.107683278C= , CM000685.1:g.107683278C= GRCh37
NC_000023.9:g.107569934C= NCBI36
NG_011977.1:g.5125C=
NG_012059.2:g.4427G=
NG_011977.2:g.5125C=

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.-78C= MANE Select ENSP00000331902.7:n.-78C=
ENST00000361603.7:c.-78C= ENSP00000354505.2:n.-78C=
ENST00000642185.1:c.-78C= ENSP00000495101.1:n.-78C=
ENST00000328300.10:c.-78C= ENSP00000331902.6:n.-78C=
ENST00000361603.6:c.-78C= ENSP00000354505.2:n.-78C=
ENST00000470339.1:n.107C=
ENST00000477429.1:n.205C=
NM_000495.4:c.-78C= NP_000486.1:n.-78C=
NM_033380.2:c.-78C= NP_203699.1:n.-78C=
XM_005262070.2:c.-78C= XP_005262127.1:n.-78C=
XM_005262072.3:c.-78C= XP_005262129.1:n.-78C=
XM_006724616.2:c.-78C= XP_006724679.1:n.-78C=
XM_011530850.1:c.-78C= XP_011529152.1:n.-78C=
NM_000495.5:c.-78C= NP_000486.1:n.-78C=
NM_033380.3:c.-78C= MANE Select NP_203699.1:n.-78C=