Canonical Allele Identifier: CA695006286

Gene: COL4A1

Linked Data

• dbSNP Id: rs1161443955
• gnomAD v3: 13-110192429-G-T
• gnomAD v4: 13-110192429-G-T
• MyVariant Identifiers: chr13:g.110844776G>T (hg19) ; chr13:g.110192429G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110192429G>T , CM000675.2:g.110192429G>T	GRCh38
NC_000013.10:g.110844776G>T , CM000675.1:g.110844776G>T	GRCh37
NC_000013.9:g.109642777G>T	NCBI36
NG_011544.2:g.119721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375820.10:c.1466-145C>A MANE Select	ENSP00000364979.4:n.1466-145C>A
ENST00000543140.6:c.1466-145C>A	ENSP00000443348.1:n.1466-145C>A
ENST00000649738.1:n.1596-145C>A
ENST00000375820.8:c.1466-145C>A	ENSP00000364979.4:n.1466-145C>A
ENST00000543140.5:c.1466-145C>A	ENSP00000443348.1:n.1466-145C>A
NM_001303110.1:c.1466-145C>A	NP_001290039.1:n.1466-145C>A
NM_001845.5:c.1466-145C>A	NP_001836.3:n.1466-145C>A
XM_011521048.1:c.1274-145C>A	XP_011519350.1:n.1274-145C>A
XM_011521048.2:c.1274-145C>A	XP_011519350.1:n.1274-145C>A
NM_001845.6:c.1466-145C>A MANE Select	NP_001836.3:n.1466-145C>A
NM_001303110.2:c.1466-145C>A	NP_001290039.1:n.1466-145C>A