Canonical Allele Identifier: CA467653298
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137642650T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134750804T>G , CM000671.2:g.134750804T>G GRCh38
NC_000009.11:g.137642650T>G , CM000671.1:g.137642650T>G GRCh37
NC_000009.10:g.136782471T>G NCBI36
NG_008030.1:g.113999T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.1584T>G ENSP00000360885.4:p.Gly528=
ENST00000371817.8:c.1584T>G MANE Select ENSP00000360882.3:p.Gly528=
ENST00000371817.7:c.1584T>G ENSP00000360882.3:p.Gly528=
ENST00000618395.4:c.1584T>G ENSP00000481360.1:p.Gly528=
NM_000093.4:c.1584T>G NP_000084.3:p.Gly528=
NM_001278074.1:c.1584T>G NP_001265003.1:p.Gly528=
XR_929712.1:n.1986T>G
XR_929713.1:n.1986T>G
XM_017014266.2:c.1584T>G XP_016869755.1:p.Gly528=
XR_001746183.1:n.1982T>G
NM_000093.5:c.1584T>G MANE Select NP_000084.3:p.Gly528=