Canonical Allele Identifier: CA2118754560

Gene: COL4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110212573C= , CM000675.2:g.110212573C=	GRCh38
NC_000013.10:g.110864920C= , CM000675.1:g.110864920C=	GRCh37
NC_000013.9:g.109662921C=	NCBI36
NG_011544.2:g.99577G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375820.10:c.324+1G= MANE Select	ENSP00000364979.4:n.324+1G=
ENST00000543140.6:c.324+1G=	ENSP00000443348.1:n.324+1G=
ENST00000615732.2:c.132+1G=	ENSP00000478222.2:n.132+1G=
ENST00000647797.1:c.203+1G=
ENST00000648170.1:n.203+1G=
ENST00000648966.1:c.203+1G=
ENST00000649484.1:c.203+1G=
ENST00000649738.1:n.454+1G=
ENST00000650138.1:n.13+1G=
ENST00000375820.8:c.324+1G=	ENSP00000364979.4:n.324+1G=
ENST00000543140.5:c.324+1G=	ENSP00000443348.1:n.324+1G=
ENST00000615732.1:c.132+1G=	ENSP00000478222.1:n.132+1G=
NM_001303110.1:c.324+1G=	NP_001290039.1:n.324+1G=
NM_001845.5:c.324+1G=	NP_001836.3:n.324+1G=
XM_011521048.1:c.132+1G=	XP_011519350.1:n.132+1G=
XM_011521048.2:c.132+1G=	XP_011519350.1:n.132+1G=
NM_001845.6:c.324+1G= MANE Select	NP_001836.3:n.324+1G=
NM_001303110.2:c.324+1G=	NP_001290039.1:n.324+1G=