Canonical Allele Identifier: CA388726411

Gene: COL4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110212461C>G , CM000675.2:g.110212461C>G	GRCh38
NC_000013.10:g.110864808C>G , CM000675.1:g.110864808C>G	GRCh37
NC_000013.9:g.109662809C>G	NCBI36
NG_011544.2:g.99689G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001845.6:c.343G>C MANE Select	NP_001836.3:p.Gly115Arg
ENST00000375820.10:c.343G>C MANE Select	ENSP00000364979.4:p.Gly115Arg
NM_001303110.1:c.343G>C	NP_001290039.1:p.Gly115Arg
NM_001303110.2:c.343G>C	NP_001290039.1:p.Gly115Arg
NM_001845.5:c.343G>C	NP_001836.3:p.Gly115Arg
ENST00000375820.8:c.343G>C	ENSP00000364979.4:p.Gly115Arg
ENST00000543140.5:c.343G>C	ENSP00000443348.1:p.Gly115Arg
ENST00000543140.6:c.343G>C	ENSP00000443348.1:p.Gly115Arg
ENST00000615732.1:c.151G>C	ENSP00000478222.1:p.Gly51Arg
ENST00000615732.2:c.151G>C	ENSP00000478222.2:p.Gly51Arg
ENST00000647797.1:c.222G>C
ENST00000648170.1:n.222G>C
ENST00000648966.1:c.222G>C
ENST00000649484.1:c.222G>C
ENST00000649738.1:n.473G>C
ENST00000650138.1:n.32G>C
XM_011521048.1:c.151G>C	XP_011519350.1:p.Gly51Arg
XM_011521048.2:c.151G>C	XP_011519350.1:p.Gly51Arg