Canonical Allele Identifier: CA2450721771

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695397A= , CM000685.2:g.108695397A=	GRCh38
NC_000023.10:g.107938627A= , CM000685.1:g.107938627A=	GRCh37
NC_000023.9:g.107825283A=	NCBI36
NG_011977.1:g.260474A=
NG_011977.2:g.260474A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4952A= MANE Select	ENSP00000331902.7:p.Tyr1651=
ENST00000361603.7:c.4934A=	ENSP00000354505.2:p.Tyr1645=
ENST00000510690.2:n.1446A=
ENST00000644079.1:n.1783A=
ENST00000328300.10:c.4952A=	ENSP00000331902.6:p.Tyr1651=
ENST00000361603.6:c.4934A=	ENSP00000354505.2:p.Tyr1645=
ENST00000504541.1:c.219+476A=	ENSP00000424845.1:n.219+476A=
ENST00000515658.1:c.325-900A=
NM_000495.4:c.4934A=	NP_000486.1:p.Tyr1645=
NM_033380.2:c.4952A=	NP_203699.1:p.Tyr1651=
XM_005262070.2:c.4943A=	XP_005262127.1:p.Tyr1648=
XM_006724616.2:c.4952A=	XP_006724679.1:p.Tyr1651=
XM_011530849.1:c.4628A=	XP_011529151.1:p.Tyr1543=
XM_011530851.1:c.2525A=	XP_011529153.1:p.Tyr842=
XM_011530849.2:c.4967A=	XP_011529151.2:p.Tyr1656=
XM_017029259.2:c.4958A=	XP_016884748.1:p.Tyr1653=
XM_017029260.1:c.4949A=	XP_016884749.1:p.Tyr1650=
XM_017029263.2:c.3287A=	XP_016884752.1:p.Tyr1096=
NM_000495.5:c.4934A=	NP_000486.1:p.Tyr1645=
NM_033380.3:c.4952A= MANE Select	NP_203699.1:p.Tyr1651=