Canonical Allele Identifier: CA7049619
Gene: COL4A2 HGNC NCBI
COL4A2-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110458888G>A , CM000675.2:g.110458888G>A GRCh38
NC_000013.10:g.111111235G>A , CM000675.1:g.111111235G>A GRCh37
NC_000013.9:g.109909236G>A NCBI36
NG_032137.1:g.156605G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360467.7:c.1550G>A (COL4A2) MANE Select ENSP00000353654.5:p.Arg517Lys
ENST00000617564.2:c.807G>A (COL4A2)
ENST00000360467.5:c.1550G>A (COL4A2) ENSP00000353654.5:p.Arg517Lys
ENST00000617564.1:c.1G>A (COL4A2)
NM_001846.2:c.1550G>A (COL4A2) NP_001837.2:p.Arg517Lys
XR_158875.3:n.620-602C>T (COL4A2-AS2)
NM_001267044.1:c.73-602C>T (COL4A2-AS2) NP_001253973.1:n.73-602C>T
NM_001846.3:c.1550G>A (COL4A2) NP_001837.2:p.Arg517Lys
NM_001846.4:c.1550G>A (COL4A2) MANE Select NP_001837.2:p.Arg517Lys
NR_171022.1:n.266-602C>T (COL4A2-AS2)