Canonical Allele Identifier: CA2450688186

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108596958_108596978delinsATTGTGTGTGTGTGTGTTTGT , CM000685.2:g.108596958_108596978delinsATTGTGTGTGTGTGTGTTTGT	GRCh38
NC_000023.10:g.107840188_107840208delinsATTGTGTGTGTGTGTGTTTGT , CM000685.1:g.107840188_107840208delinsATTGTGTGTGTGTGTGTTTGT	GRCh37
NC_000023.9:g.107726844_107726864delinsATTGTGTGTGTGTGTGTTTGT	NCBI36
NG_011977.1:g.162035_162055delinsATTGTGTGTGTGTGTGTTTGT
NG_011977.2:g.162035_162055delinsATTGTGTGTGTGTGTGTTTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT MANE Select	ENSP00000331902.7:n.1517-40_1517-20delins...
ENST00000361603.7:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	ENSP00000354505.2:n.1517-40_1517-20delins...
ENST00000328300.10:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	ENSP00000331902.6:n.1517-40_1517-20delins...
ENST00000361603.6:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	ENSP00000354505.2:n.1517-40_1517-20delins...
ENST00000483338.1:n.973-40_973-20delinsATTGTGTGTGTGTGTGTTTGT
NM_000495.4:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	NP_000486.1:n.1517-40_1517-20delinsATTGTG...
NM_033380.2:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	NP_203699.1:n.1517-40_1517-20delinsATTGTG...
XM_005262070.2:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	XP_005262127.1:n.1517-40_1517-20delinsATT...
XM_005262072.3:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	XP_005262129.1:n.1517-40_1517-20delinsATT...
XM_006724616.2:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	XP_006724679.1:n.1517-40_1517-20delinsATT...
XM_011530849.1:c.1193-40_1193-20delinsATTGTGTGTGTGTGTGTTTGT	XP_011529151.1:n.1193-40_1193-20delinsATT...
XM_011530850.1:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	XP_011529152.1:n.1517-40_1517-20delinsATT...
XM_011530849.2:c.1532-40_1532-20delinsATTGTGTGTGTGTGTGTTTGT	XP_011529151.2:n.1532-40_1532-20delinsATT...
XM_017029259.2:c.1532-40_1532-20delinsATTGTGTGTGTGTGTGTTTGT	XP_016884748.1:n.1532-40_1532-20delinsATT...
XM_017029260.1:c.1532-40_1532-20delinsATTGTGTGTGTGTGTGTTTGT	XP_016884749.1:n.1532-40_1532-20delinsATT...
XM_017029261.1:c.1532-40_1532-20delinsATTGTGTGTGTGTGTGTTTGT	XP_016884750.1:n.1532-40_1532-20delinsATT...
XM_017029262.2:c.1532-40_1532-20delinsATTGTGTGTGTGTGTGTTTGT	XP_016884751.1:n.1532-40_1532-20delinsATT...
XM_017029263.2:c.-149-40_-149-20delinsATTGTGTGTGTGTGTGTTTGT	XP_016884752.1:n.-149-40_-149-20delinsATT...
NM_000495.5:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT	NP_000486.1:n.1517-40_1517-20delinsATTGTG...
NM_033380.3:c.1517-40_1517-20delinsATTGTGTGTGTGTGTGTTTGT MANE Select	NP_203699.1:n.1517-40_1517-20delinsATTGTG...