Canonical Allele Identifier: CA2694439013

Gene: COL4A5

Linked Data

• gnomAD v4: X-108539886-GCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108539889_108539891del , CM000685.2:g.108539889_108539891del	GRCh38
NC_000023.10:g.107783119_107783121del , CM000685.1:g.107783119_107783121del	GRCh37
NC_000023.9:g.107669775_107669777del	NCBI36
NG_011977.1:g.104966_104968del
NG_011977.2:g.104966_104968del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.141+84_141+86del MANE Select	ENSP00000331902.7:n.141+84_141+86del
ENST00000361603.7:c.141+84_141+86del	ENSP00000354505.2:n.141+84_141+86del
ENST00000328300.10:c.141+84_141+86del	ENSP00000331902.6:n.141+84_141+86del
ENST00000361603.6:c.141+84_141+86del	ENSP00000354505.2:n.141+84_141+86del
ENST00000470339.1:n.325+84_325+86del
NM_000495.4:c.141+84_141+86del	NP_000486.1:n.141+84_141+86del
NM_033380.2:c.141+84_141+86del	NP_203699.1:n.141+84_141+86del
XM_005262070.2:c.141+84_141+86del	XP_005262127.1:n.141+84_141+86del
XM_005262072.3:c.141+84_141+86del	XP_005262129.1:n.141+84_141+86del
XM_006724616.2:c.141+84_141+86del	XP_006724679.1:n.141+84_141+86del
XM_011530849.1:c.-184+84_-184+86del	XP_011529151.1:n.-184+84_-184+86del
XM_011530850.1:c.141+84_141+86del	XP_011529152.1:n.141+84_141+86del
XM_011530849.2:c.156+84_156+86del	XP_011529151.2:n.156+84_156+86del
XM_017029259.2:c.156+84_156+86del	XP_016884748.1:n.156+84_156+86del
XM_017029260.1:c.156+84_156+86del	XP_016884749.1:n.156+84_156+86del
XM_017029261.1:c.156+84_156+86del	XP_016884750.1:n.156+84_156+86del
XM_017029262.2:c.156+84_156+86del	XP_016884751.1:n.156+84_156+86del
NM_000495.5:c.141+84_141+86del	NP_000486.1:n.141+84_141+86del
NM_033380.3:c.141+84_141+86del MANE Select	NP_203699.1:n.141+84_141+86del