Canonical Allele Identifier: CA643637307

Gene: COL4A5

Linked Data

• dbSNP Id: rs1379365148
• gnomAD v2: X-107937941-C-A
• gnomAD v3: X-108694711-C-A
• gnomAD v4: X-108694711-C-A
• MyVariant Identifiers: chrX:g.107937941C>A (hg19) ; chrX:g.108694711C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694711C>A , CM000685.2:g.108694711C>A	GRCh38
NC_000023.10:g.107937941C>A , CM000685.1:g.107937941C>A	GRCh37
NC_000023.9:g.107824597C>A	NCBI36
NG_011977.1:g.259788C>A
NG_011977.2:g.259788C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4707-96C>A MANE Select	ENSP00000331902.7:n.4707-96C>A
ENST00000361603.7:c.4689-96C>A	ENSP00000354505.2:n.4689-96C>A
ENST00000510690.2:n.1201-96C>A
ENST00000644079.1:n.1097C>A
ENST00000328300.10:c.4707-96C>A	ENSP00000331902.6:n.4707-96C>A
ENST00000361603.6:c.4689-96C>A	ENSP00000354505.2:n.4689-96C>A
ENST00000504541.1:c.105-96C>A	ENSP00000424845.1:n.105-96C>A
ENST00000515658.1:c.325-1586C>A
NM_000495.4:c.4689-96C>A	NP_000486.1:n.4689-96C>A
NM_033380.2:c.4707-96C>A	NP_203699.1:n.4707-96C>A
XM_005262070.2:c.4698-96C>A	XP_005262127.1:n.4698-96C>A
XM_006724616.2:c.4707-96C>A	XP_006724679.1:n.4707-96C>A
XM_011530849.1:c.4383-96C>A	XP_011529151.1:n.4383-96C>A
XM_011530851.1:c.2280-96C>A	XP_011529153.1:n.2280-96C>A
XM_011530849.2:c.4722-96C>A	XP_011529151.2:n.4722-96C>A
XM_017029259.2:c.4713-96C>A	XP_016884748.1:n.4713-96C>A
XM_017029260.1:c.4704-96C>A	XP_016884749.1:n.4704-96C>A
XM_017029263.2:c.3042-96C>A	XP_016884752.1:n.3042-96C>A
NM_000495.5:c.4689-96C>A	NP_000486.1:n.4689-96C>A
NM_033380.3:c.4707-96C>A MANE Select	NP_203699.1:n.4707-96C>A