Canonical Allele Identifier: CA1136194836

Gene: COL4A5

Linked Data

• dbSNP Id: rs2068532116
• gnomAD v3: X-108685833-A-G
• gnomAD v4: X-108685833-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108685833A>G , CM000685.2:g.108685833A>G	GRCh38
NC_000023.10:g.107929063A>G , CM000685.1:g.107929063A>G	GRCh37
NC_000023.9:g.107815719A>G	NCBI36
NG_011977.1:g.250910A>G
NG_011977.2:g.250910A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4217-198A>G MANE Select	ENSP00000331902.7:n.4217-198A>G
ENST00000361603.7:c.4199-198A>G	ENSP00000354505.2:n.4199-198A>G
ENST00000510690.2:n.711-198A>G
ENST00000328300.10:c.4217-198A>G	ENSP00000331902.6:n.4217-198A>G
ENST00000361603.6:c.4199-198A>G	ENSP00000354505.2:n.4199-198A>G
ENST00000489230.1:n.620-198A>G
ENST00000515658.1:c.13-198A>G
NM_000495.4:c.4199-198A>G	NP_000486.1:n.4199-198A>G
NM_033380.2:c.4217-198A>G	NP_203699.1:n.4217-198A>G
XM_005262070.2:c.4208-198A>G	XP_005262127.1:n.4208-198A>G
XM_006724616.2:c.4217-198A>G	XP_006724679.1:n.4217-198A>G
XM_011530849.1:c.3893-198A>G	XP_011529151.1:n.3893-198A>G
XM_011530851.1:c.1790-198A>G	XP_011529153.1:n.1790-198A>G
XM_011530849.2:c.4232-198A>G	XP_011529151.2:n.4232-198A>G
XM_017029259.2:c.4223-198A>G	XP_016884748.1:n.4223-198A>G
XM_017029260.1:c.4214-198A>G	XP_016884749.1:n.4214-198A>G
XM_017029263.2:c.2552-198A>G	XP_016884752.1:n.2552-198A>G
NM_000495.5:c.4199-198A>G	NP_000486.1:n.4199-198A>G
NM_033380.3:c.4217-198A>G MANE Select	NP_203699.1:n.4217-198A>G