Canonical Allele Identifier: CA414132785

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938566C>A (hg19) ; chrX:g.108695336C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695336C>A , CM000685.2:g.108695336C>A	GRCh38
NC_000023.10:g.107938566C>A , CM000685.1:g.107938566C>A	GRCh37
NC_000023.9:g.107825222C>A	NCBI36
NG_011977.1:g.260413C>A
NG_011977.2:g.260413C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4891C>A MANE Select	ENSP00000331902.7:p.Arg1631Ser
ENST00000361603.7:c.4873C>A	ENSP00000354505.2:p.Arg1625Ser
ENST00000510690.2:n.1385C>A
ENST00000644079.1:n.1722C>A
ENST00000328300.10:c.4891C>A	ENSP00000331902.6:p.Arg1631Ser
ENST00000361603.6:c.4873C>A	ENSP00000354505.2:p.Arg1625Ser
ENST00000504541.1:c.219+415C>A	ENSP00000424845.1:n.219+415C>A
ENST00000515658.1:c.325-961C>A
NM_000495.4:c.4873C>A	NP_000486.1:p.Arg1625Ser
NM_033380.2:c.4891C>A	NP_203699.1:p.Arg1631Ser
XM_005262070.2:c.4882C>A	XP_005262127.1:p.Arg1628Ser
XM_006724616.2:c.4891C>A	XP_006724679.1:p.Arg1631Ser
XM_011530849.1:c.4567C>A	XP_011529151.1:p.Arg1523Ser
XM_011530851.1:c.2464C>A	XP_011529153.1:p.Arg822Ser
XM_011530849.2:c.4906C>A	XP_011529151.2:p.Arg1636Ser
XM_017029259.2:c.4897C>A	XP_016884748.1:p.Arg1633Ser
XM_017029260.1:c.4888C>A	XP_016884749.1:p.Arg1630Ser
XM_017029263.2:c.3226C>A	XP_016884752.1:p.Arg1076Ser
NM_000495.5:c.4873C>A	NP_000486.1:p.Arg1625Ser
NM_033380.3:c.4891C>A MANE Select	NP_203699.1:p.Arg1631Ser