Canonical Allele Identifier: CA2694414017
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108584429A>G , CM000685.2:g.108584429A>G GRCh38
NC_000023.10:g.107827659A>G , CM000685.1:g.107827659A>G GRCh37
NC_000023.9:g.107714315A>G NCBI36
NG_011977.1:g.149506A>G
NG_011977.2:g.149506A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.991-55A>G MANE Select ENSP00000331902.7:n.991-55A>G
ENST00000361603.7:c.991-55A>G ENSP00000354505.2:n.991-55A>G
ENST00000328300.10:c.991-55A>G ENSP00000331902.6:n.991-55A>G
ENST00000361603.6:c.991-55A>G ENSP00000354505.2:n.991-55A>G
ENST00000483338.1:n.447-55A>G
NM_000495.4:c.991-55A>G NP_000486.1:n.991-55A>G
NM_033380.2:c.991-55A>G NP_203699.1:n.991-55A>G
XM_005262070.2:c.991-55A>G XP_005262127.1:n.991-55A>G
XM_005262072.3:c.991-55A>G XP_005262129.1:n.991-55A>G
XM_006724616.2:c.991-55A>G XP_006724679.1:n.991-55A>G
XM_011530849.1:c.667-55A>G XP_011529151.1:n.667-55A>G
XM_011530850.1:c.991-55A>G XP_011529152.1:n.991-55A>G
XM_011530849.2:c.1006-55A>G XP_011529151.2:n.1006-55A>G
XM_017029259.2:c.1006-55A>G XP_016884748.1:n.1006-55A>G
XM_017029260.1:c.1006-55A>G XP_016884749.1:n.1006-55A>G
XM_017029261.1:c.1006-55A>G XP_016884750.1:n.1006-55A>G
XM_017029262.2:c.1006-55A>G XP_016884751.1:n.1006-55A>G
XM_017029263.2:c.-719-55A>G XP_016884752.1:n.-719-55A>G
NM_000495.5:c.991-55A>G NP_000486.1:n.991-55A>G
NM_033380.3:c.991-55A>G MANE Select NP_203699.1:n.991-55A>G