Canonical Allele Identifier: CA2514612559

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108570758del , CM000685.2:g.108570758del	GRCh38
NC_000023.10:g.107813988del , CM000685.1:g.107813988del	GRCh37
NC_000023.9:g.107700644del	NCBI36
NG_011977.1:g.135835del
NG_011977.2:g.135835del

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.385-655del MANE Select	ENSP00000331902.7:n.385-655del
ENST00000361603.7:c.385-655del	ENSP00000354505.2:n.385-655del
ENST00000328300.10:c.385-655del	ENSP00000331902.6:n.385-655del
ENST00000361603.6:c.385-655del	ENSP00000354505.2:n.385-655del
NM_000495.4:c.385-655del	NP_000486.1:n.385-655del
NM_033380.2:c.385-655del	NP_203699.1:n.385-655del
XM_005262070.2:c.385-655del	XP_005262127.1:n.385-655del
XM_005262072.3:c.385-655del	XP_005262129.1:n.385-655del
XM_006724616.2:c.385-655del	XP_006724679.1:n.385-655del
XM_011530849.1:c.61-655del	XP_011529151.1:n.61-655del
XM_011530850.1:c.385-655del	XP_011529152.1:n.385-655del
XM_011530849.2:c.400-655del	XP_011529151.2:n.400-655del
XM_017029259.2:c.400-655del	XP_016884748.1:n.400-655del
XM_017029260.1:c.400-655del	XP_016884749.1:n.400-655del
XM_017029261.1:c.400-655del	XP_016884750.1:n.400-655del
XM_017029262.2:c.400-655del	XP_016884751.1:n.400-655del
NM_000495.5:c.385-655del	NP_000486.1:n.385-655del
NM_033380.3:c.385-655del MANE Select	NP_203699.1:n.385-655del