Canonical Allele Identifier: CA643629482

Gene: COL4A5

Linked Data

• ClinVar Variation Id: 3022113
• ClinVar RCV Id: RCV003881192
• dbSNP Id: rs1311059217
• gnomAD v2: X-107840310-G-A
• gnomAD v3: X-108597080-G-A
• gnomAD v4: X-108597080-G-A
• MyVariant Identifiers: chrX:g.107840310G>A (hg19) ; chrX:g.108597080G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108597080G>A , CM000685.2:g.108597080G>A	GRCh38
NC_000023.10:g.107840310G>A , CM000685.1:g.107840310G>A	GRCh37
NC_000023.9:g.107726966G>A	NCBI36
NG_011977.1:g.162157G>A
NG_011977.2:g.162157G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.1587+12G>A MANE Select	ENSP00000331902.7:n.1587+12G>A
ENST00000361603.7:c.1587+12G>A	ENSP00000354505.2:n.1587+12G>A
ENST00000328300.10:c.1587+12G>A	ENSP00000331902.6:n.1587+12G>A
ENST00000361603.6:c.1587+12G>A	ENSP00000354505.2:n.1587+12G>A
ENST00000483338.1:n.1043+12G>A
NM_000495.4:c.1587+12G>A	NP_000486.1:n.1587+12G>A
NM_033380.2:c.1587+12G>A	NP_203699.1:n.1587+12G>A
XM_005262070.2:c.1587+12G>A	XP_005262127.1:n.1587+12G>A
XM_005262072.3:c.1587+12G>A	XP_005262129.1:n.1587+12G>A
XM_006724616.2:c.1587+12G>A	XP_006724679.1:n.1587+12G>A
XM_011530849.1:c.1263+12G>A	XP_011529151.1:n.1263+12G>A
XM_011530850.1:c.1587+12G>A	XP_011529152.1:n.1587+12G>A
XM_011530849.2:c.1602+12G>A	XP_011529151.2:n.1602+12G>A
XM_017029259.2:c.1602+12G>A	XP_016884748.1:n.1602+12G>A
XM_017029260.1:c.1602+12G>A	XP_016884749.1:n.1602+12G>A
XM_017029261.1:c.1602+12G>A	XP_016884750.1:n.1602+12G>A
XM_017029262.2:c.1602+12G>A	XP_016884751.1:n.1602+12G>A
XM_017029263.2:c.-79+12G>A	XP_016884752.1:n.-79+12G>A
NM_000495.5:c.1587+12G>A	NP_000486.1:n.1587+12G>A
NM_033380.3:c.1587+12G>A MANE Select	NP_203699.1:n.1587+12G>A