Canonical Allele Identifier: CA2579675660

Gene: COL4A5

Linked Data

• gnomAD v4: X-108440232-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108440235del , CM000685.2:g.108440235del	GRCh38
NC_000023.10:g.107683465del , CM000685.1:g.107683465del	GRCh37
NC_000023.9:g.107570121del	NCBI36
NG_011977.1:g.5312del
NG_012059.2:g.4242del
NG_011977.2:g.5312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.81+29del MANE Select	ENSP00000331902.7:n.81+29del
ENST00000361603.7:c.81+29del	ENSP00000354505.2:n.81+29del
ENST00000642185.1:c.81+29del	ENSP00000495101.1:n.81+29del
ENST00000328300.10:c.81+29del	ENSP00000331902.6:n.81+29del
ENST00000361603.6:c.81+29del	ENSP00000354505.2:n.81+29del
ENST00000470339.1:n.265+29del
ENST00000477429.1:n.363+29del
NM_000495.4:c.81+29del	NP_000486.1:n.81+29del
NM_033380.2:c.81+29del	NP_203699.1:n.81+29del
XM_005262070.2:c.81+29del	XP_005262127.1:n.81+29del
XM_005262072.3:c.81+29del	XP_005262129.1:n.81+29del
XM_006724616.2:c.81+29del	XP_006724679.1:n.81+29del
XM_011530850.1:c.81+29del	XP_011529152.1:n.81+29del
NM_000495.5:c.81+29del	NP_000486.1:n.81+29del
NM_033380.3:c.81+29del MANE Select	NP_203699.1:n.81+29del