Canonical Allele Identifier: CA2450721517

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694668G= , CM000685.2:g.108694668G=	GRCh38
NC_000023.10:g.107937898G= , CM000685.1:g.107937898G=	GRCh37
NC_000023.9:g.107824554G=	NCBI36
NG_011977.1:g.259745G=
NG_011977.2:g.259745G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4707-139G= MANE Select	ENSP00000331902.7:n.4707-139G=
ENST00000361603.7:c.4689-139G=	ENSP00000354505.2:n.4689-139G=
ENST00000510690.2:n.1201-139G=
ENST00000644079.1:n.1054G=
ENST00000328300.10:c.4707-139G=	ENSP00000331902.6:n.4707-139G=
ENST00000361603.6:c.4689-139G=	ENSP00000354505.2:n.4689-139G=
ENST00000504541.1:c.105-139G=	ENSP00000424845.1:n.105-139G=
ENST00000515658.1:c.325-1629G=
NM_000495.4:c.4689-139G=	NP_000486.1:n.4689-139G=
NM_033380.2:c.4707-139G=	NP_203699.1:n.4707-139G=
XM_005262070.2:c.4698-139G=	XP_005262127.1:n.4698-139G=
XM_006724616.2:c.4707-139G=	XP_006724679.1:n.4707-139G=
XM_011530849.1:c.4383-139G=	XP_011529151.1:n.4383-139G=
XM_011530851.1:c.2280-139G=	XP_011529153.1:n.2280-139G=
XM_011530849.2:c.4722-139G=	XP_011529151.2:n.4722-139G=
XM_017029259.2:c.4713-139G=	XP_016884748.1:n.4713-139G=
XM_017029260.1:c.4704-139G=	XP_016884749.1:n.4704-139G=
XM_017029263.2:c.3042-139G=	XP_016884752.1:n.3042-139G=
NM_000495.5:c.4689-139G=	NP_000486.1:n.4689-139G=
NM_033380.3:c.4707-139G= MANE Select	NP_203699.1:n.4707-139G=