Canonical Allele Identifier: CA388726523

Gene: COL4A1

Linked Data

• MyVariant Identifiers: chr13:g.110864923G>T (hg19) ; chr13:g.110212576G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110212576G>T , CM000675.2:g.110212576G>T	GRCh38
NC_000013.10:g.110864923G>T , CM000675.1:g.110864923G>T	GRCh37
NC_000013.9:g.109662924G>T	NCBI36
NG_011544.2:g.99574C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375820.10:c.322C>A MANE Select	ENSP00000364979.4:p.Pro108Thr
ENST00000543140.6:c.322C>A	ENSP00000443348.1:p.Pro108Thr
ENST00000615732.2:c.130C>A	ENSP00000478222.2:p.Pro44Thr
ENST00000647797.1:c.201C>A
ENST00000648170.1:n.201C>A
ENST00000648966.1:c.201C>A
ENST00000649484.1:c.201C>A
ENST00000649738.1:n.452C>A
ENST00000650138.1:n.11C>A
ENST00000375820.8:c.322C>A	ENSP00000364979.4:p.Pro108Thr
ENST00000543140.5:c.322C>A	ENSP00000443348.1:p.Pro108Thr
ENST00000615732.1:c.130C>A	ENSP00000478222.1:p.Pro44Thr
NM_001303110.1:c.322C>A	NP_001290039.1:p.Pro108Thr
NM_001845.5:c.322C>A	NP_001836.3:p.Pro108Thr
XM_011521048.1:c.130C>A	XP_011519350.1:p.Pro44Thr
XM_011521048.2:c.130C>A	XP_011519350.1:p.Pro44Thr
NM_001845.6:c.322C>A MANE Select	NP_001836.3:p.Pro108Thr
NM_001303110.2:c.322C>A	NP_001290039.1:p.Pro108Thr