Canonical Allele Identifier: CA2450719180

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687449T= , CM000685.2:g.108687449T=	GRCh38
NC_000023.10:g.107930679T= , CM000685.1:g.107930679T=	GRCh37
NC_000023.9:g.107817335T=	NCBI36
NG_011977.1:g.252526T=
NG_011977.2:g.252526T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4316-33T= MANE Select	ENSP00000331902.7:n.4316-33T=
ENST00000361603.7:c.4298-33T=	ENSP00000354505.2:n.4298-33T=
ENST00000510690.2:n.810-33T=
ENST00000328300.10:c.4316-33T=	ENSP00000331902.6:n.4316-33T=
ENST00000361603.6:c.4298-33T=	ENSP00000354505.2:n.4298-33T=
ENST00000489230.1:n.719-33T=
ENST00000515658.1:c.112-33T=
NM_000495.4:c.4298-33T=	NP_000486.1:n.4298-33T=
NM_033380.2:c.4316-33T=	NP_203699.1:n.4316-33T=
XM_005262070.2:c.4307-33T=	XP_005262127.1:n.4307-33T=
XM_006724616.2:c.4316-33T=	XP_006724679.1:n.4316-33T=
XM_011530849.1:c.3992-33T=	XP_011529151.1:n.3992-33T=
XM_011530851.1:c.1889-33T=	XP_011529153.1:n.1889-33T=
XM_011530849.2:c.4331-33T=	XP_011529151.2:n.4331-33T=
XM_017029259.2:c.4322-33T=	XP_016884748.1:n.4322-33T=
XM_017029260.1:c.4313-33T=	XP_016884749.1:n.4313-33T=
XM_017029263.2:c.2651-33T=	XP_016884752.1:n.2651-33T=
NM_000495.5:c.4298-33T=	NP_000486.1:n.4298-33T=
NM_033380.3:c.4316-33T= MANE Select	NP_203699.1:n.4316-33T=