Canonical Allele Identifier: CA2694413592

Gene: COL4A5

Linked Data

• gnomAD v4: X-108601770-A-ATCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108601770_108601771insTCCG , CM000685.2:g.108601770_108601771insTCCG	GRCh38
NC_000023.10:g.107845000_107845001insTCCG , CM000685.1:g.107845000_107845001insTCCG	GRCh37
NC_000023.9:g.107731656_107731657insTCCG	NCBI36
NG_011977.1:g.166847_166848insTCCG
NG_011977.2:g.166847_166848insTCCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.2042-115_2042-114insTCCG MANE Select	ENSP00000331902.7:n.2042-115_2042-114insTCCG
ENST00000361603.7:c.2042-115_2042-114insTCCG	ENSP00000354505.2:n.2042-115_2042-114insTCCG
ENST00000328300.10:c.2042-115_2042-114insTCCG	ENSP00000331902.6:n.2042-115_2042-114insTCCG
ENST00000361603.6:c.2042-115_2042-114insTCCG	ENSP00000354505.2:n.2042-115_2042-114insTCCG
ENST00000483338.1:n.1498-115_1498-114insTCCG
NM_000495.4:c.2042-115_2042-114insTCCG	NP_000486.1:n.2042-115_2042-114insTCCG
NM_033380.2:c.2042-115_2042-114insTCCG	NP_203699.1:n.2042-115_2042-114insTCCG
XM_005262070.2:c.2042-115_2042-114insTCCG	XP_005262127.1:n.2042-115_2042-114insTCCG
XM_005262072.3:c.2042-115_2042-114insTCCG	XP_005262129.1:n.2042-115_2042-114insTCCG
XM_006724616.2:c.2042-115_2042-114insTCCG	XP_006724679.1:n.2042-115_2042-114insTCCG
XM_011530849.1:c.1718-115_1718-114insTCCG	XP_011529151.1:n.1718-115_1718-114insTCCG
XM_011530850.1:c.2042-115_2042-114insTCCG	XP_011529152.1:n.2042-115_2042-114insTCCG
XM_011530849.2:c.2057-115_2057-114insTCCG	XP_011529151.2:n.2057-115_2057-114insTCCG
XM_017029259.2:c.2057-115_2057-114insTCCG	XP_016884748.1:n.2057-115_2057-114insTCCG
XM_017029260.1:c.2057-115_2057-114insTCCG	XP_016884749.1:n.2057-115_2057-114insTCCG
XM_017029261.1:c.2057-115_2057-114insTCCG	XP_016884750.1:n.2057-115_2057-114insTCCG
XM_017029262.2:c.2057-115_2057-114insTCCG	XP_016884751.1:n.2057-115_2057-114insTCCG
XM_017029263.2:c.377-115_377-114insTCCG	XP_016884752.1:n.377-115_377-114insTCCG
NM_000495.5:c.2042-115_2042-114insTCCG	NP_000486.1:n.2042-115_2042-114insTCCG
NM_033380.3:c.2042-115_2042-114insTCCG MANE Select	NP_203699.1:n.2042-115_2042-114insTCCG