Canonical Allele Identifier: CA2450686550

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108591546_108591549delinsCTTT , CM000685.2:g.108591546_108591549delinsCTTT	GRCh38
NC_000023.10:g.107834776_107834779delinsCTTT , CM000685.1:g.107834776_107834779delinsCTTT	GRCh37
NC_000023.9:g.107721432_107721435delinsCTTT	NCBI36
NG_011977.1:g.156623_156626delinsCTTT
NG_011977.2:g.156623_156626delinsCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.1340-15_1340-12delinsCTTT MANE Select	ENSP00000331902.7:n.1340-15_1340-12delins...
ENST00000361603.7:c.1340-15_1340-12delinsCTTT	ENSP00000354505.2:n.1340-15_1340-12delins...
ENST00000328300.10:c.1340-15_1340-12delinsCTTT	ENSP00000331902.6:n.1340-15_1340-12delins...
ENST00000361603.6:c.1340-15_1340-12delinsCTTT	ENSP00000354505.2:n.1340-15_1340-12delins...
ENST00000483338.1:n.796-15_796-12delinsCTTT
NM_000495.4:c.1340-15_1340-12delinsCTTT	NP_000486.1:n.1340-15_1340-12delinsCTTT
NM_033380.2:c.1340-15_1340-12delinsCTTT	NP_203699.1:n.1340-15_1340-12delinsCTTT
XM_005262070.2:c.1340-15_1340-12delinsCTTT	XP_005262127.1:n.1340-15_1340-12delinsCTT...
XM_005262072.3:c.1340-15_1340-12delinsCTTT	XP_005262129.1:n.1340-15_1340-12delinsCTT...
XM_006724616.2:c.1340-15_1340-12delinsCTTT	XP_006724679.1:n.1340-15_1340-12delinsCTT...
XM_011530849.1:c.1016-15_1016-12delinsCTTT	XP_011529151.1:n.1016-15_1016-12delinsCTT...
XM_011530850.1:c.1340-15_1340-12delinsCTTT	XP_011529152.1:n.1340-15_1340-12delinsCTT...
XM_011530849.2:c.1355-15_1355-12delinsCTTT	XP_011529151.2:n.1355-15_1355-12delinsCTT...
XM_017029259.2:c.1355-15_1355-12delinsCTTT	XP_016884748.1:n.1355-15_1355-12delinsCTT...
XM_017029260.1:c.1355-15_1355-12delinsCTTT	XP_016884749.1:n.1355-15_1355-12delinsCTT...
XM_017029261.1:c.1355-15_1355-12delinsCTTT	XP_016884750.1:n.1355-15_1355-12delinsCTT...
XM_017029262.2:c.1355-15_1355-12delinsCTTT	XP_016884751.1:n.1355-15_1355-12delinsCTT...
XM_017029263.2:c.-370-15_-370-12delinsCTTT	XP_016884752.1:n.-370-15_-370-12delinsCTT...
NM_000495.5:c.1340-15_1340-12delinsCTTT	NP_000486.1:n.1340-15_1340-12delinsCTTT
NM_033380.3:c.1340-15_1340-12delinsCTTT MANE Select	NP_203699.1:n.1340-15_1340-12delinsCTTT