Canonical Allele Identifier: CA467666794
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137726861G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134835015G>A , CM000671.2:g.134835015G>A GRCh38
NC_000009.11:g.137726861G>A , CM000671.1:g.137726861G>A GRCh37
NC_000009.10:g.136866682G>A NCBI36
NG_008030.1:g.198210G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.5181G>A ENSP00000360885.4:p.Gln1727=
ENST00000371817.8:c.5181G>A MANE Select ENSP00000360882.3:p.Gln1727=
ENST00000371817.7:c.5181G>A ENSP00000360882.3:p.Gln1727=
ENST00000371820.3:c.439G>A
ENST00000618395.4:c.5181G>A ENSP00000481360.1:p.Gln1727=
NM_000093.4:c.5181G>A NP_000084.3:p.Gln1727=
NM_001278074.1:c.5181G>A NP_001265003.1:p.Gln1727=
NR_103451.2:n.71-14806C>T
XR_929712.1:n.5865G>A
XR_929713.1:n.5733G>A
NM_000093.5:c.5181G>A MANE Select NP_000084.3:p.Gln1727=