Canonical Allele Identifier: CA2450698032

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108626126_108626128delinsCTT , CM000685.2:g.108626126_108626128delinsCTT	GRCh38
NC_000023.10:g.107869356_107869358delinsCTT , CM000685.1:g.107869356_107869358delinsCTT	GRCh37
NC_000023.9:g.107756012_107756014delinsCTT	NCBI36
NG_011977.1:g.191203_191205delinsCTT
NG_011977.2:g.191203_191205delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.3107-84_3107-82delinsCTT MANE Select	ENSP00000331902.7:n.3107-84_3107-82delins...
ENST00000361603.7:c.3107-84_3107-82delinsCTT	ENSP00000354505.2:n.3107-84_3107-82delins...
ENST00000328300.10:c.3107-84_3107-82delinsCTT	ENSP00000331902.6:n.3107-84_3107-82delins...
ENST00000361603.6:c.3107-84_3107-82delinsCTT	ENSP00000354505.2:n.3107-84_3107-82delins...
ENST00000483338.1:n.2563-84_2563-82delinsCTT
ENST00000505728.1:c.340-84_340-82delinsCTT
NM_000495.4:c.3107-84_3107-82delinsCTT	NP_000486.1:n.3107-84_3107-82delinsCTT
NM_033380.2:c.3107-84_3107-82delinsCTT	NP_203699.1:n.3107-84_3107-82delinsCTT
XM_005262070.2:c.3107-84_3107-82delinsCTT	XP_005262127.1:n.3107-84_3107-82delinsCTT...
XM_005262072.3:c.3107-84_3107-82delinsCTT	XP_005262129.1:n.3107-84_3107-82delinsCTT...
XM_006724616.2:c.3107-84_3107-82delinsCTT	XP_006724679.1:n.3107-84_3107-82delinsCTT...
XM_011530849.1:c.2783-84_2783-82delinsCTT	XP_011529151.1:n.2783-84_2783-82delinsCTT...
XM_011530850.1:c.3107-84_3107-82delinsCTT	XP_011529152.1:n.3107-84_3107-82delinsCTT...
XM_011530851.1:c.680-84_680-82delinsCTT	XP_011529153.1:n.680-84_680-82delinsCTT
XM_011530849.2:c.3122-84_3122-82delinsCTT	XP_011529151.2:n.3122-84_3122-82delinsCTT...
XM_017029259.2:c.3122-84_3122-82delinsCTT	XP_016884748.1:n.3122-84_3122-82delinsCTT...
XM_017029260.1:c.3122-84_3122-82delinsCTT	XP_016884749.1:n.3122-84_3122-82delinsCTT...
XM_017029261.1:c.3122-84_3122-82delinsCTT	XP_016884750.1:n.3122-84_3122-82delinsCTT...
XM_017029262.2:c.3122-84_3122-82delinsCTT	XP_016884751.1:n.3122-84_3122-82delinsCTT...
XM_017029263.2:c.1442-84_1442-82delinsCTT	XP_016884752.1:n.1442-84_1442-82delinsCTT...
NM_000495.5:c.3107-84_3107-82delinsCTT	NP_000486.1:n.3107-84_3107-82delinsCTT
NM_033380.3:c.3107-84_3107-82delinsCTT MANE Select	NP_203699.1:n.3107-84_3107-82delinsCTT