Canonical Allele Identifier: CA869813588

Gene: COL4A5

Linked Data

• dbSNP Id: rs746121814
• gnomAD v4: X-108620210-C-A
• MyVariant Identifiers: chrX:g.107863440C>A (hg19) ; chrX:g.108620210C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108620210C>A , CM000685.2:g.108620210C>A	GRCh38
NC_000023.10:g.107863440C>A , CM000685.1:g.107863440C>A	GRCh37
NC_000023.9:g.107750096C>A	NCBI36
NG_011977.1:g.185287C>A
NG_011977.2:g.185287C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.2510-49C>A MANE Select	ENSP00000331902.7:n.2510-49C>A
ENST00000361603.7:c.2510-49C>A	ENSP00000354505.2:n.2510-49C>A
ENST00000328300.10:c.2510-49C>A	ENSP00000331902.6:n.2510-49C>A
ENST00000361603.6:c.2510-49C>A	ENSP00000354505.2:n.2510-49C>A
ENST00000483338.1:n.1966-49C>A
NM_000495.4:c.2510-49C>A	NP_000486.1:n.2510-49C>A
NM_033380.2:c.2510-49C>A	NP_203699.1:n.2510-49C>A
XM_005262070.2:c.2510-49C>A	XP_005262127.1:n.2510-49C>A
XM_005262072.3:c.2510-49C>A	XP_005262129.1:n.2510-49C>A
XM_006724616.2:c.2510-49C>A	XP_006724679.1:n.2510-49C>A
XM_011530849.1:c.2186-49C>A	XP_011529151.1:n.2186-49C>A
XM_011530850.1:c.2510-49C>A	XP_011529152.1:n.2510-49C>A
XM_011530851.1:c.83-49C>A	XP_011529153.1:n.83-49C>A
XM_011530849.2:c.2525-49C>A	XP_011529151.2:n.2525-49C>A
XM_017029259.2:c.2525-49C>A	XP_016884748.1:n.2525-49C>A
XM_017029260.1:c.2525-49C>A	XP_016884749.1:n.2525-49C>A
XM_017029261.1:c.2525-49C>A	XP_016884750.1:n.2525-49C>A
XM_017029262.2:c.2525-49C>A	XP_016884751.1:n.2525-49C>A
XM_017029263.2:c.845-49C>A	XP_016884752.1:n.845-49C>A
NM_000495.5:c.2510-49C>A	NP_000486.1:n.2510-49C>A
NM_033380.3:c.2510-49C>A MANE Select	NP_203699.1:n.2510-49C>A