Canonical Allele Identifier: CA2450721605

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694902T= , CM000685.2:g.108694902T=	GRCh38
NC_000023.10:g.107938132T= , CM000685.1:g.107938132T=	GRCh37
NC_000023.9:g.107824788T=	NCBI36
NG_011977.1:g.259979T=
NG_011977.2:g.259979T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4802T= MANE Select	ENSP00000331902.7:p.Ile1601=
ENST00000361603.7:c.4784T=	ENSP00000354505.2:p.Ile1595=
ENST00000510690.2:n.1296T=
ENST00000644079.1:n.1288T=
ENST00000328300.10:c.4802T=	ENSP00000331902.6:p.Ile1601=
ENST00000361603.6:c.4784T=	ENSP00000354505.2:p.Ile1595=
ENST00000504541.1:c.200T=	ENSP00000424845.1:p.Ile67=
ENST00000515658.1:c.325-1395T=
NM_000495.4:c.4784T=	NP_000486.1:p.Ile1595=
NM_033380.2:c.4802T=	NP_203699.1:p.Ile1601=
XM_005262070.2:c.4793T=	XP_005262127.1:p.Ile1598=
XM_006724616.2:c.4802T=	XP_006724679.1:p.Ile1601=
XM_011530849.1:c.4478T=	XP_011529151.1:p.Ile1493=
XM_011530851.1:c.2375T=	XP_011529153.1:p.Ile792=
XM_011530849.2:c.4817T=	XP_011529151.2:p.Ile1606=
XM_017029259.2:c.4808T=	XP_016884748.1:p.Ile1603=
XM_017029260.1:c.4799T=	XP_016884749.1:p.Ile1600=
XM_017029263.2:c.3137T=	XP_016884752.1:p.Ile1046=
NM_000495.5:c.4784T=	NP_000486.1:p.Ile1595=
NM_033380.3:c.4802T= MANE Select	NP_203699.1:p.Ile1601=