Canonical Allele Identifier: CA2450688191

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108596961_108596979delinsGTGTGTGTGTGTGTTTGTT , CM000685.2:g.108596961_108596979delinsGTGTGTGTGTGTGTTTGTT	GRCh38
NC_000023.10:g.107840191_107840209delinsGTGTGTGTGTGTGTTTGTT , CM000685.1:g.107840191_107840209delinsGTGTGTGTGTGTGTTTGTT	GRCh37
NC_000023.9:g.107726847_107726865delinsGTGTGTGTGTGTGTTTGTT	NCBI36
NG_011977.1:g.162038_162056delinsGTGTGTGTGTGTGTTTGTT
NG_011977.2:g.162038_162056delinsGTGTGTGTGTGTGTTTGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT MANE Select	ENSP00000331902.7:n.1517-37_1517-19delins...
ENST00000361603.7:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	ENSP00000354505.2:n.1517-37_1517-19delins...
ENST00000328300.10:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	ENSP00000331902.6:n.1517-37_1517-19delins...
ENST00000361603.6:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	ENSP00000354505.2:n.1517-37_1517-19delins...
ENST00000483338.1:n.973-37_973-19delinsGTGTGTGTGTGTGTTTGTT
NM_000495.4:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	NP_000486.1:n.1517-37_1517-19delinsGTGTGT...
NM_033380.2:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	NP_203699.1:n.1517-37_1517-19delinsGTGTGT...
XM_005262070.2:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	XP_005262127.1:n.1517-37_1517-19delinsGTG...
XM_005262072.3:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	XP_005262129.1:n.1517-37_1517-19delinsGTG...
XM_006724616.2:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	XP_006724679.1:n.1517-37_1517-19delinsGTG...
XM_011530849.1:c.1193-37_1193-19delinsGTGTGTGTGTGTGTTTGTT	XP_011529151.1:n.1193-37_1193-19delinsGTG...
XM_011530850.1:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	XP_011529152.1:n.1517-37_1517-19delinsGTG...
XM_011530849.2:c.1532-37_1532-19delinsGTGTGTGTGTGTGTTTGTT	XP_011529151.2:n.1532-37_1532-19delinsGTG...
XM_017029259.2:c.1532-37_1532-19delinsGTGTGTGTGTGTGTTTGTT	XP_016884748.1:n.1532-37_1532-19delinsGTG...
XM_017029260.1:c.1532-37_1532-19delinsGTGTGTGTGTGTGTTTGTT	XP_016884749.1:n.1532-37_1532-19delinsGTG...
XM_017029261.1:c.1532-37_1532-19delinsGTGTGTGTGTGTGTTTGTT	XP_016884750.1:n.1532-37_1532-19delinsGTG...
XM_017029262.2:c.1532-37_1532-19delinsGTGTGTGTGTGTGTTTGTT	XP_016884751.1:n.1532-37_1532-19delinsGTG...
XM_017029263.2:c.-149-37_-149-19delinsGTGTGTGTGTGTGTTTGTT	XP_016884752.1:n.-149-37_-149-19delinsGTG...
NM_000495.5:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT	NP_000486.1:n.1517-37_1517-19delinsGTGTGT...
NM_033380.3:c.1517-37_1517-19delinsGTGTGTGTGTGTGTTTGTT MANE Select	NP_203699.1:n.1517-37_1517-19delinsGTGTGT...