Canonical Allele Identifier: CA2694415570

Gene: COL4A5

Linked Data

• gnomAD v4: X-108695151-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695153_108695154del , CM000685.2:g.108695153_108695154del	GRCh38
NC_000023.10:g.107938383_107938384del , CM000685.1:g.107938383_107938384del	GRCh37
NC_000023.9:g.107825039_107825040del	NCBI36
NG_011977.1:g.260230_260231del
NG_011977.2:g.260230_260231del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4822-114_4822-113del MANE Select	ENSP00000331902.7:n.4822-114_4822-113del
ENST00000361603.7:c.4804-114_4804-113del	ENSP00000354505.2:n.4804-114_4804-113del
ENST00000510690.2:n.1316-114_1316-113del
ENST00000644079.1:n.1539_1540del
ENST00000328300.10:c.4822-114_4822-113del	ENSP00000331902.6:n.4822-114_4822-113del
ENST00000361603.6:c.4804-114_4804-113del	ENSP00000354505.2:n.4804-114_4804-113del
ENST00000504541.1:c.219+232_219+233del	ENSP00000424845.1:n.219+232_219+233del
ENST00000515658.1:c.325-1144_325-1143del
NM_000495.4:c.4804-114_4804-113del	NP_000486.1:n.4804-114_4804-113del
NM_033380.2:c.4822-114_4822-113del	NP_203699.1:n.4822-114_4822-113del
XM_005262070.2:c.4813-114_4813-113del	XP_005262127.1:n.4813-114_4813-113del
XM_006724616.2:c.4822-114_4822-113del	XP_006724679.1:n.4822-114_4822-113del
XM_011530849.1:c.4498-114_4498-113del	XP_011529151.1:n.4498-114_4498-113del
XM_011530851.1:c.2395-114_2395-113del	XP_011529153.1:n.2395-114_2395-113del
XM_011530849.2:c.4837-114_4837-113del	XP_011529151.2:n.4837-114_4837-113del
XM_017029259.2:c.4828-114_4828-113del	XP_016884748.1:n.4828-114_4828-113del
XM_017029260.1:c.4819-114_4819-113del	XP_016884749.1:n.4819-114_4819-113del
XM_017029263.2:c.3157-114_3157-113del	XP_016884752.1:n.3157-114_3157-113del
NM_000495.5:c.4804-114_4804-113del	NP_000486.1:n.4804-114_4804-113del
NM_033380.3:c.4822-114_4822-113del MANE Select	NP_203699.1:n.4822-114_4822-113del