Canonical Allele Identifier: CA430442426
Gene: COL5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189899741G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189035015G>A , CM000664.2:g.189035015G>A GRCh38
NC_000002.11:g.189899741G>A , CM000664.1:g.189899741G>A GRCh37
NC_000002.10:g.189607986G>A NCBI36
NG_011799.1:g.149865C>T
NG_011799.2:g.149865C>T
NG_011799.3:g.195287C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.4254C>T MANE Select ENSP00000364000.3:p.Asn1418=
ENST00000374866.7:c.4254C>T ENSP00000364000.3:p.Asn1418=
ENST00000618828.1:c.3093C>T ENSP00000482184.1:p.Asn1031=
NM_000393.3:c.4254C>T NP_000384.2:p.Asn1418=
XM_011510573.1:c.4116C>T XP_011508875.1:p.Asn1372=
NM_000393.4:c.4254C>T NP_000384.2:p.Asn1418=
XM_011510573.3:c.4116C>T XP_011508875.1:p.Asn1372=
NM_000393.5:c.4254C>T MANE Select NP_000384.2:p.Asn1418=