Canonical Allele Identifier: CA413852233

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107925067C>G (hg19) ; chrX:g.108681837C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108681837C>G , CM000685.2:g.108681837C>G	GRCh38
NC_000023.10:g.107925067C>G , CM000685.1:g.107925067C>G	GRCh37
NC_000023.9:g.107811723C>G	NCBI36
NG_011977.1:g.246914C>G
NG_011977.2:g.246914C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4165C>G MANE Select	ENSP00000331902.7:p.Gln1389Glu
ENST00000361603.7:c.4147C>G	ENSP00000354505.2:p.Gln1383Glu
ENST00000510690.2:n.659C>G
ENST00000328300.10:c.4165C>G	ENSP00000331902.6:p.Gln1389Glu
ENST00000361603.6:c.4147C>G	ENSP00000354505.2:p.Gln1383Glu
ENST00000489230.1:n.568C>G
NM_000495.4:c.4147C>G	NP_000486.1:p.Gln1383Glu
NM_033380.2:c.4165C>G	NP_203699.1:p.Gln1389Glu
XM_005262070.2:c.4156C>G	XP_005262127.1:p.Gln1386Glu
XM_006724616.2:c.4165C>G	XP_006724679.1:p.Gln1389Glu
XM_011530849.1:c.3841C>G	XP_011529151.1:p.Gln1281Glu
XM_011530851.1:c.1738C>G	XP_011529153.1:p.Gln580Glu
XM_011530849.2:c.4180C>G	XP_011529151.2:p.Gln1394Glu
XM_017029259.2:c.4171C>G	XP_016884748.1:p.Gln1391Glu
XM_017029260.1:c.4162C>G	XP_016884749.1:p.Gln1388Glu
XM_017029263.2:c.2500C>G	XP_016884752.1:p.Gln834Glu
NM_000495.5:c.4147C>G	NP_000486.1:p.Gln1383Glu
NM_033380.3:c.4165C>G MANE Select	NP_203699.1:p.Gln1389Glu