Canonical Allele Identifier: CA15776494

Gene: COL4A2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110378231A>G , CM000675.2:g.110378231A>G	GRCh38
NC_000013.10:g.111030578A>G , CM000675.1:g.111030578A>G	GRCh37
NC_000013.9:g.109828579A>G	NCBI36
NG_032137.1:g.75948A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360467.7:c.180+20679A>G MANE Select	ENSP00000353654.5:n.180+20679A>G
ENST00000400163.7:c.180+20679A>G	ENSP00000383027.3:n.180+20679A>G
ENST00000650540.1:c.180+20679A>G	ENSP00000497878.1:n.180+20679A>G
ENST00000360467.5:c.180+20679A>G	ENSP00000353654.5:n.180+20679A>G
ENST00000400163.6:c.180+20679A>G	ENSP00000383027.2:n.180+20679A>G
NM_001846.2:c.180+20679A>G	NP_001837.2:n.180+20679A>G
NM_001846.3:c.180+20679A>G	NP_001837.2:n.180+20679A>G
NM_001846.4:c.180+20679A>G MANE Select	NP_001837.2:n.180+20679A>G