Canonical Allele Identifier: CA388724667

Gene: COL4A1

Linked Data

• gnomAD v4: 13-110205385-A-T
• MyVariant Identifiers: chr13:g.110857732A>T (hg19) ; chr13:g.110205385A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110205385A>T , CM000675.2:g.110205385A>T	GRCh38
NC_000013.10:g.110857732A>T , CM000675.1:g.110857732A>T	GRCh37
NC_000013.9:g.109655733A>T	NCBI36
NG_011544.2:g.106765T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375820.10:c.925T>A MANE Select	ENSP00000364979.4:p.Tyr309Asn
ENST00000543140.6:c.925T>A	ENSP00000443348.1:p.Tyr309Asn
ENST00000647632.1:n.558T>A
ENST00000647797.1:c.804T>A
ENST00000649738.1:n.1055T>A
ENST00000375820.8:c.925T>A	ENSP00000364979.4:p.Tyr309Asn
ENST00000543140.5:c.925T>A	ENSP00000443348.1:p.Tyr309Asn
NM_001303110.1:c.925T>A	NP_001290039.1:p.Tyr309Asn
NM_001845.5:c.925T>A	NP_001836.3:p.Tyr309Asn
XM_011521048.1:c.733T>A	XP_011519350.1:p.Tyr245Asn
XM_011521048.2:c.733T>A	XP_011519350.1:p.Tyr245Asn
NM_001845.6:c.925T>A MANE Select	NP_001836.3:p.Tyr309Asn
NM_001303110.2:c.925T>A	NP_001290039.1:p.Tyr309Asn