Canonical Allele Identifier: CA13838648
Gene: COL4A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110357296G>A , CM000675.2:g.110357296G>A GRCh38
NC_000013.10:g.111009643G>A , CM000675.1:g.111009643G>A GRCh37
NC_000013.9:g.109807644G>A NCBI36
NG_032137.1:g.55013G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001846.4:c.100-176G>A MANE Select NP_001837.2:n.100-176G>A
ENST00000360467.7:c.100-176G>A MANE Select ENSP00000353654.5:n.100-176G>A
NM_001846.2:c.100-176G>A NP_001837.2:n.100-176G>A
NM_001846.3:c.100-176G>A NP_001837.2:n.100-176G>A
ENST00000360467.5:c.100-176G>A ENSP00000353654.5:n.100-176G>A
ENST00000400163.6:c.100-176G>A ENSP00000383027.2:n.100-176G>A
ENST00000400163.7:c.100-176G>A ENSP00000383027.3:n.100-176G>A
ENST00000649101.1:c.100-176G>A ENSP00000497869.1:n.100-176G>A
ENST00000650540.1:c.100-176G>A ENSP00000497878.1:n.100-176G>A