Canonical Allele Identifier: CA388725385

Gene: COL4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110209409C>G , CM000675.2:g.110209409C>G	GRCh38
NC_000013.10:g.110861756C>G , CM000675.1:g.110861756C>G	GRCh37
NC_000013.9:g.109659757C>G	NCBI36
NG_011544.2:g.102741G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001845.6:c.634G>C MANE Select	NP_001836.3:p.Gly212Arg
ENST00000375820.10:c.634G>C MANE Select	ENSP00000364979.4:p.Gly212Arg
NM_001303110.1:c.634G>C	NP_001290039.1:p.Gly212Arg
NM_001303110.2:c.634G>C	NP_001290039.1:p.Gly212Arg
NM_001845.5:c.634G>C	NP_001836.3:p.Gly212Arg
ENST00000375820.8:c.634G>C	ENSP00000364979.4:p.Gly212Arg
ENST00000543140.5:c.634G>C	ENSP00000443348.1:p.Gly212Arg
ENST00000543140.6:c.634G>C	ENSP00000443348.1:p.Gly212Arg
ENST00000615732.1:c.442G>C	ENSP00000478222.1:p.Gly148Arg
ENST00000615732.2:c.442G>C	ENSP00000478222.2:p.Gly148Arg
ENST00000647632.1:n.267G>C
ENST00000647797.1:c.513G>C
ENST00000649738.1:n.764G>C
XM_011521048.1:c.442G>C	XP_011519350.1:p.Gly148Arg
XM_011521048.2:c.442G>C	XP_011519350.1:p.Gly148Arg