Canonical Allele Identifier: CA467652865
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137582783T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134690937T>A , CM000671.2:g.134690937T>A GRCh38
NC_000009.11:g.137582783T>A , CM000671.1:g.137582783T>A GRCh37
NC_000009.10:g.136722604T>A NCBI36
NG_008030.1:g.54132T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371820.4:c.135T>A ENSP00000360885.4:p.Val45=
ENST00000371817.8:c.135T>A MANE Select ENSP00000360882.3:p.Val45=
ENST00000371817.7:c.135T>A ENSP00000360882.3:p.Val45=
ENST00000464187.1:n.321T>A
ENST00000618395.4:c.135T>A ENSP00000481360.1:p.Val45=
NM_000093.4:c.135T>A NP_000084.3:p.Val45=
NM_001278074.1:c.135T>A NP_001265003.1:p.Val45=
XR_929712.1:n.537T>A
XR_929713.1:n.537T>A
XM_017014266.2:c.135T>A XP_016869755.1:p.Val45=
XR_001746183.1:n.533T>A
NM_000093.5:c.135T>A MANE Select NP_000084.3:p.Val45=