Canonical Allele Identifier: CA256269038

Gene: COL4A1

Linked Data

• dbSNP Id: rs909563880
• gnomAD v4: 13-110192147-C-A
• MyVariant Identifiers: chr13:g.110844494C>A (hg19) ; chr13:g.110192147C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110192147C>A , CM000675.2:g.110192147C>A	GRCh38
NC_000013.10:g.110844494C>A , CM000675.1:g.110844494C>A	GRCh37
NC_000013.9:g.109642495C>A	NCBI36
NG_011544.2:g.120003G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375820.10:c.1536+67G>T MANE Select	ENSP00000364979.4:n.1536+67G>T
ENST00000543140.6:c.1536+67G>T	ENSP00000443348.1:n.1536+67G>T
ENST00000649738.1:n.1666+67G>T
ENST00000375820.8:c.1536+67G>T	ENSP00000364979.4:n.1536+67G>T
ENST00000543140.5:c.1536+67G>T	ENSP00000443348.1:n.1536+67G>T
NM_001303110.1:c.1536+67G>T	NP_001290039.1:n.1536+67G>T
NM_001845.5:c.1536+67G>T	NP_001836.3:n.1536+67G>T
XM_011521048.1:c.1344+67G>T	XP_011519350.1:n.1344+67G>T
XM_011521048.2:c.1344+67G>T	XP_011519350.1:n.1344+67G>T
NM_001845.6:c.1536+67G>T MANE Select	NP_001836.3:n.1536+67G>T
NM_001303110.2:c.1536+67G>T	NP_001290039.1:n.1536+67G>T