Canonical Allele Identifier: CA413851102
Gene: COL4A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108680890A>G , CM000685.2:g.108680890A>G GRCh38
NC_000023.10:g.107924120A>G , CM000685.1:g.107924120A>G GRCh37
NC_000023.9:g.107810776A>G NCBI36
NG_011977.1:g.245967A>G
NG_011977.2:g.245967A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.4021A>G MANE Select ENSP00000331902.7:p.Lys1341Glu
ENST00000361603.7:c.4003A>G ENSP00000354505.2:p.Lys1335Glu
ENST00000510690.2:n.515A>G
ENST00000328300.10:c.4021A>G ENSP00000331902.6:p.Lys1341Glu
ENST00000361603.6:c.4003A>G ENSP00000354505.2:p.Lys1335Glu
ENST00000489230.1:n.424A>G
NM_000495.4:c.4003A>G NP_000486.1:p.Lys1335Glu
NM_033380.2:c.4021A>G NP_203699.1:p.Lys1341Glu
XM_005262070.2:c.4012A>G XP_005262127.1:p.Lys1338Glu
XM_006724616.2:c.4021A>G XP_006724679.1:p.Lys1341Glu
XM_011530849.1:c.3697A>G XP_011529151.1:p.Lys1233Glu
XM_011530851.1:c.1594A>G XP_011529153.1:p.Lys532Glu
XM_011530849.2:c.4036A>G XP_011529151.2:p.Lys1346Glu
XM_017029259.2:c.4027A>G XP_016884748.1:p.Lys1343Glu
XM_017029260.1:c.4018A>G XP_016884749.1:p.Lys1340Glu
XM_017029263.2:c.2356A>G XP_016884752.1:p.Lys786Glu
NM_000495.5:c.4003A>G NP_000486.1:p.Lys1335Glu
NM_033380.3:c.4021A>G MANE Select NP_203699.1:p.Lys1341Glu