Canonical Allele Identifier: CA2450680237

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108571813_108571814delinsAC , CM000685.2:g.108571813_108571814delinsAC	GRCh38
NC_000023.10:g.107815043_107815044delinsAC , CM000685.1:g.107815043_107815044delinsAC	GRCh37
NC_000023.9:g.107701699_107701700delinsAC	NCBI36
NG_011977.1:g.136890_136891delinsAC
NG_011977.2:g.136890_136891delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.441_442delinsAC MANE Select	ENSP00000331902.7:p.Gly147=
ENST00000361603.7:c.441_442delinsAC	ENSP00000354505.2:p.Gly147=
ENST00000328300.10:c.441_442delinsAC	ENSP00000331902.6:p.Gly147=
ENST00000361603.6:c.441_442delinsAC	ENSP00000354505.2:p.Gly147=
NM_000495.4:c.441_442delinsAC	NP_000486.1:p.Gly147=
NM_033380.2:c.441_442delinsAC	NP_203699.1:p.Gly147=
XM_005262070.2:c.441_442delinsAC	XP_005262127.1:p.Gly147=
XM_005262072.3:c.441_442delinsAC	XP_005262129.1:p.Gly147=
XM_006724616.2:c.441_442delinsAC	XP_006724679.1:p.Gly147=
XM_011530849.1:c.117_118delinsAC	XP_011529151.1:p.Gly39=
XM_011530850.1:c.441_442delinsAC	XP_011529152.1:p.Gly147=
XM_011530849.2:c.456_457delinsAC	XP_011529151.2:p.Gly152=
XM_017029259.2:c.456_457delinsAC	XP_016884748.1:p.Gly152=
XM_017029260.1:c.456_457delinsAC	XP_016884749.1:p.Gly152=
XM_017029261.1:c.456_457delinsAC	XP_016884750.1:p.Gly152=
XM_017029262.2:c.456_457delinsAC	XP_016884751.1:p.Gly152=
NM_000495.5:c.441_442delinsAC	NP_000486.1:p.Gly147=
NM_033380.3:c.441_442delinsAC MANE Select	NP_203699.1:p.Gly147=