Canonical Allele Identifier: CA2118754604

Gene: COL4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110212666C= , CM000675.2:g.110212666C=	GRCh38
NC_000013.10:g.110865013C= , CM000675.1:g.110865013C=	GRCh37
NC_000013.9:g.109663014C=	NCBI36
NG_011544.2:g.99484G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375820.10:c.280-48G= MANE Select	ENSP00000364979.4:n.280-48G=
ENST00000543140.6:c.280-48G=	ENSP00000443348.1:n.280-48G=
ENST00000615732.2:c.88-48G=	ENSP00000478222.2:n.88-48G=
ENST00000647797.1:c.159-48G=
ENST00000648170.1:n.159-48G=
ENST00000648966.1:c.159-48G=
ENST00000649484.1:c.159-48G=
ENST00000649738.1:n.410-48G=
ENST00000375820.8:c.280-48G=	ENSP00000364979.4:n.280-48G=
ENST00000543140.5:c.280-48G=	ENSP00000443348.1:n.280-48G=
ENST00000615732.1:c.88-48G=	ENSP00000478222.1:n.88-48G=
NM_001303110.1:c.280-48G=	NP_001290039.1:n.280-48G=
NM_001845.5:c.280-48G=	NP_001836.3:n.280-48G=
XM_011521048.1:c.88-48G=	XP_011519350.1:n.88-48G=
XM_011521048.2:c.88-48G=	XP_011519350.1:n.88-48G=
NM_001845.6:c.280-48G= MANE Select	NP_001836.3:n.280-48G=
NM_001303110.2:c.280-48G=	NP_001290039.1:n.280-48G=