Canonical Allele Identifier: CA2694415754

Gene: COL4A5

Linked Data

• gnomAD v4: X-108695859-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695859_108695860insA , CM000685.2:g.108695859_108695860insA	GRCh38
NC_000023.10:g.107939089_107939090insA , CM000685.1:g.107939089_107939090insA	GRCh37
NC_000023.9:g.107825745_107825746insA	NCBI36
NG_011977.1:g.260936_260937insA
NG_011977.2:g.260936_260937insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4994+420_4994+421insA MANE Select	ENSP00000331902.7:n.4994+420_4994+421insA
ENST00000361603.7:c.4976+420_4976+421insA	ENSP00000354505.2:n.4976+420_4976+421insA
ENST00000510690.2:n.1488+420_1488+421insA
ENST00000644079.1:n.2245_2246insA
ENST00000328300.10:c.4994+420_4994+421insA	ENSP00000331902.6:n.4994+420_4994+421insA
ENST00000361603.6:c.4976+420_4976+421insA	ENSP00000354505.2:n.4976+420_4976+421insA
ENST00000504541.1:c.220-438_220-437insA	ENSP00000424845.1:n.220-438_220-437insA
ENST00000515658.1:c.325-438_325-437insA
NM_000495.4:c.4976+420_4976+421insA	NP_000486.1:n.4976+420_4976+421insA
NM_033380.2:c.4994+420_4994+421insA	NP_203699.1:n.4994+420_4994+421insA
XM_005262070.2:c.4985+420_4985+421insA	XP_005262127.1:n.4985+420_4985+421insA
XM_006724616.2:c.4994+420_4994+421insA	XP_006724679.1:n.4994+420_4994+421insA
XM_011530849.1:c.4670+420_4670+421insA	XP_011529151.1:n.4670+420_4670+421insA
XM_011530851.1:c.2567+420_2567+421insA	XP_011529153.1:n.2567+420_2567+421insA
XM_011530849.2:c.5009+420_5009+421insA	XP_011529151.2:n.5009+420_5009+421insA
XM_017029259.2:c.5000+420_5000+421insA	XP_016884748.1:n.5000+420_5000+421insA
XM_017029260.1:c.4991+420_4991+421insA	XP_016884749.1:n.4991+420_4991+421insA
XM_017029263.2:c.3329+420_3329+421insA	XP_016884752.1:n.3329+420_3329+421insA
NM_000495.5:c.4976+420_4976+421insA	NP_000486.1:n.4976+420_4976+421insA
NM_033380.3:c.4994+420_4994+421insA MANE Select	NP_203699.1:n.4994+420_4994+421insA