Canonical Allele Identifier: CA388726479

Gene: COL4A1

Linked Data

• MyVariant Identifiers: chr13:g.110864827C>A (hg19) ; chr13:g.110212480C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110212480C>A , CM000675.2:g.110212480C>A	GRCh38
NC_000013.10:g.110864827C>A , CM000675.1:g.110864827C>A	GRCh37
NC_000013.9:g.109662828C>A	NCBI36
NG_011544.2:g.99670G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375820.10:c.325-1G>T MANE Select	ENSP00000364979.4:n.325-1G>T
ENST00000543140.6:c.325-1G>T	ENSP00000443348.1:n.325-1G>T
ENST00000615732.2:c.133-1G>T	ENSP00000478222.2:n.133-1G>T
ENST00000647797.1:c.204-1G>T
ENST00000648170.1:n.204-1G>T
ENST00000648966.1:c.204-1G>T
ENST00000649484.1:c.204-1G>T
ENST00000649738.1:n.455-1G>T
ENST00000650138.1:n.14-1G>T
ENST00000375820.8:c.325-1G>T	ENSP00000364979.4:n.325-1G>T
ENST00000543140.5:c.325-1G>T	ENSP00000443348.1:n.325-1G>T
ENST00000615732.1:c.133-1G>T	ENSP00000478222.1:n.133-1G>T
NM_001303110.1:c.325-1G>T	NP_001290039.1:n.325-1G>T
NM_001845.5:c.325-1G>T	NP_001836.3:n.325-1G>T
XM_011521048.1:c.133-1G>T	XP_011519350.1:n.133-1G>T
XM_011521048.2:c.133-1G>T	XP_011519350.1:n.133-1G>T
NM_001845.6:c.325-1G>T MANE Select	NP_001836.3:n.325-1G>T
NM_001303110.2:c.325-1G>T	NP_001290039.1:n.325-1G>T