Canonical Allele Identifier: CA7048553
Community Standard Title: NM_001845.6(COL4A1):c.343G>A (p.Gly115Ser)
Gene: COL4A1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_001845.6:c.343G>A MANE Select NP_001836.3:p.Gly115Ser
ENST00000375820.10:c.343G>A MANE Select ENSP00000364979.4:p.Gly115Ser
NM_001303110.1:c.343G>A NP_001290039.1:p.Gly115Ser
NM_001303110.2:c.343G>A NP_001290039.1:p.Gly115Ser
NM_001845.5:c.343G>A NP_001836.3:p.Gly115Ser
ENST00000375820.8:c.343G>A ENSP00000364979.4:p.Gly115Ser
ENST00000543140.5:c.343G>A ENSP00000443348.1:p.Gly115Ser
ENST00000543140.6:c.343G>A ENSP00000443348.1:p.Gly115Ser
ENST00000615732.1:c.151G>A ENSP00000478222.1:p.Gly51Ser
ENST00000615732.2:c.151G>A ENSP00000478222.2:p.Gly51Ser
ENST00000647797.1:c.222G>A
ENST00000648170.1:n.222G>A
ENST00000648966.1:c.222G>A
ENST00000649484.1:c.222G>A
ENST00000649738.1:n.473G>A
ENST00000650138.1:n.32G>A
XM_011521048.1:c.151G>A XP_011519350.1:p.Gly51Ser
XM_011521048.2:c.151G>A XP_011519350.1:p.Gly51Ser