Canonical Allele Identifier: CA1136184825

Gene: COL4A5

Linked Data

• dbSNP Id: rs2064367662
• gnomAD v3: X-108439958-C-CA
• gnomAD v4: X-108439958-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108439958_108439959insA , CM000685.2:g.108439958_108439959insA	GRCh38
NC_000023.10:g.107683188_107683189insA , CM000685.1:g.107683188_107683189insA	GRCh37
NC_000023.9:g.107569844_107569845insA	NCBI36
NG_011977.1:g.5035_5036insA
NG_012059.2:g.4516_4517insT
NG_011977.2:g.5035_5036insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.-168_-167insA MANE Select	ENSP00000331902.7:n.-168_-167insA
ENST00000361603.7:c.-168_-167insA	ENSP00000354505.2:n.-168_-167insA
ENST00000642185.1:c.-168_-167insA	ENSP00000495101.1:n.-168_-167insA
ENST00000328300.10:c.-168_-167insA	ENSP00000331902.6:n.-168_-167insA
ENST00000361603.6:c.-168_-167insA	ENSP00000354505.2:n.-168_-167insA
ENST00000470339.1:n.17_18insA
ENST00000477429.1:n.115_116insA
NM_000495.4:c.-168_-167insA	NP_000486.1:n.-168_-167insA
NM_033380.2:c.-168_-167insA	NP_203699.1:n.-168_-167insA
XM_005262070.2:c.-168_-167insA	XP_005262127.1:n.-168_-167insA
XM_005262072.3:c.-168_-167insA	XP_005262129.1:n.-168_-167insA
XM_006724616.2:c.-120-48_-120-47insA	XP_006724679.1:n.-120-48_-120-47insA
XM_011530850.1:c.-168_-167insA	XP_011529152.1:n.-168_-167insA
NM_000495.5:c.-168_-167insA	NP_000486.1:n.-168_-167insA
NM_033380.3:c.-168_-167insA MANE Select	NP_203699.1:n.-168_-167insA