Canonical Allele Identifier: CA2740029352

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108626510T>G , CM000685.2:g.108626510T>G	GRCh38
NC_000023.10:g.107869740T>G , CM000685.1:g.107869740T>G	GRCh37
NC_000023.9:g.107756396T>G	NCBI36
NG_011977.1:g.191587T>G
NG_011977.2:g.191587T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.3246+161T>G MANE Select	ENSP00000331902.7:n.3246+161T>G
ENST00000361603.7:c.3246+161T>G	ENSP00000354505.2:n.3246+161T>G
ENST00000328300.10:c.3246+161T>G	ENSP00000331902.6:n.3246+161T>G
ENST00000361603.6:c.3246+161T>G	ENSP00000354505.2:n.3246+161T>G
ENST00000483338.1:n.2863T>G
ENST00000505728.1:c.492T>G
NM_000495.4:c.3246+161T>G	NP_000486.1:n.3246+161T>G
NM_033380.2:c.3246+161T>G	NP_203699.1:n.3246+161T>G
XM_005262070.2:c.3246+161T>G	XP_005262127.1:n.3246+161T>G
XM_005262072.3:c.3259T>G	XP_005262129.1:p.Tyr1087Asp
XM_006724616.2:c.3246+161T>G	XP_006724679.1:n.3246+161T>G
XM_011530849.1:c.2922+161T>G	XP_011529151.1:n.2922+161T>G
XM_011530850.1:c.3246+161T>G	XP_011529152.1:n.3246+161T>G
XM_011530851.1:c.819+161T>G	XP_011529153.1:n.819+161T>G
XM_011530849.2:c.3261+161T>G	XP_011529151.2:n.3261+161T>G
XM_017029259.2:c.3261+161T>G	XP_016884748.1:n.3261+161T>G
XM_017029260.1:c.3261+161T>G	XP_016884749.1:n.3261+161T>G
XM_017029261.1:c.3261+161T>G	XP_016884750.1:n.3261+161T>G
XM_017029262.2:c.3261+161T>G	XP_016884751.1:n.3261+161T>G
XM_017029263.2:c.1581+161T>G	XP_016884752.1:n.1581+161T>G
NM_000495.5:c.3246+161T>G	NP_000486.1:n.3246+161T>G
NM_033380.3:c.3246+161T>G MANE Select	NP_203699.1:n.3246+161T>G