Canonical Allele Identifier: CA2450634578

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108439927G= , CM000685.2:g.108439927G=	GRCh38
NC_000023.10:g.107683157G= , CM000685.1:g.107683157G=	GRCh37
NC_000023.9:g.107569813G=	NCBI36
NG_011977.1:g.5004G=
NG_012059.2:g.4548C=
NG_011977.2:g.5004G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.-199G= MANE Select	ENSP00000331902.7:n.-199G=
ENST00000361603.7:c.-199G=	ENSP00000354505.2:n.-199G=
ENST00000642185.1:c.-199G=	ENSP00000495101.1:n.-199G=
ENST00000328300.10:c.-199G=	ENSP00000331902.6:n.-199G=
ENST00000361603.6:c.-199G=	ENSP00000354505.2:n.-199G=
ENST00000477429.1:n.84G=
NM_000495.4:c.-199G=	NP_000486.1:n.-199G=
NM_033380.2:c.-199G=	NP_203699.1:n.-199G=
XM_005262070.2:c.-199G=	XP_005262127.1:n.-199G=
XM_005262072.3:c.-199G=	XP_005262129.1:n.-199G=
XM_006724616.2:c.-120-79G=	XP_006724679.1:n.-120-79G=
XM_011530850.1:c.-199G=	XP_011529152.1:n.-199G=
NM_000495.5:c.-199G=	NP_000486.1:n.-199G=
NM_033380.3:c.-199G= MANE Select	NP_203699.1:n.-199G=