Canonical Allele Identifier: CA388727026

Gene: COL4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110213933C>G , CM000675.2:g.110213933C>G	GRCh38
NC_000013.10:g.110866280C>G , CM000675.1:g.110866280C>G	GRCh37
NC_000013.9:g.109664281C>G	NCBI36
NG_011544.2:g.98217G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001845.6:c.227G>C MANE Select	NP_001836.3:p.Gly76Ala
ENST00000375820.10:c.227G>C MANE Select	ENSP00000364979.4:p.Gly76Ala
NM_001303110.1:c.227G>C	NP_001290039.1:p.Gly76Ala
NM_001303110.2:c.227G>C	NP_001290039.1:p.Gly76Ala
NM_001845.5:c.227G>C	NP_001836.3:p.Gly76Ala
ENST00000375820.8:c.227G>C	ENSP00000364979.4:p.Gly76Ala
ENST00000543140.5:c.227G>C	ENSP00000443348.1:p.Gly76Ala
ENST00000543140.6:c.227G>C	ENSP00000443348.1:p.Gly76Ala
ENST00000615732.1:c.35G>C	ENSP00000478222.1:p.Gly12Ala
ENST00000615732.2:c.35G>C	ENSP00000478222.2:p.Gly12Ala
ENST00000647797.1:c.106G>C
ENST00000648170.1:n.106G>C
ENST00000648966.1:c.106G>C
ENST00000649484.1:c.106G>C
ENST00000649738.1:n.357G>C
XM_011521048.1:c.35G>C	XP_011519350.1:p.Gly12Ala
XM_011521048.2:c.35G>C	XP_011519350.1:p.Gly12Ala