Canonical Allele Identifier: CA430442428
Gene: COL5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189899747A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189035021A>G , CM000664.2:g.189035021A>G GRCh38
NC_000002.11:g.189899747A>G , CM000664.1:g.189899747A>G GRCh37
NC_000002.10:g.189607992A>G NCBI36
NG_011799.1:g.149859T>C
NG_011799.2:g.149859T>C
NG_011799.3:g.195281T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.4248T>C MANE Select ENSP00000364000.3:p.Ala1416=
ENST00000374866.7:c.4248T>C ENSP00000364000.3:p.Ala1416=
ENST00000618828.1:c.3087T>C ENSP00000482184.1:p.Ala1029=
NM_000393.3:c.4248T>C NP_000384.2:p.Ala1416=
XM_011510573.1:c.4110T>C XP_011508875.1:p.Ala1370=
NM_000393.4:c.4248T>C NP_000384.2:p.Ala1416=
XM_011510573.3:c.4110T>C XP_011508875.1:p.Ala1370=
NM_000393.5:c.4248T>C MANE Select NP_000384.2:p.Ala1416=