Canonical Allele Identifier: CA467654489
Gene: COL5A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.137591792T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134699946T>A , CM000671.2:g.134699946T>A GRCh38
NC_000009.11:g.137591792T>A , CM000671.1:g.137591792T>A GRCh37
NC_000009.10:g.136731613T>A NCBI36
NG_008030.1:g.63141T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371820.4:c.315T>A ENSP00000360885.4:p.Thr105=
ENST00000371817.8:c.315T>A MANE Select ENSP00000360882.3:p.Thr105=
ENST00000371817.7:c.315T>A ENSP00000360882.3:p.Thr105=
ENST00000464187.1:n.737T>A
ENST00000618395.4:c.315T>A ENSP00000481360.1:p.Thr105=
NM_000093.4:c.315T>A NP_000084.3:p.Thr105=
NM_001278074.1:c.315T>A NP_001265003.1:p.Thr105=
XR_929712.1:n.717T>A
XR_929713.1:n.717T>A
XM_017014266.2:c.315T>A XP_016869755.1:p.Thr105=
XR_001746183.1:n.713T>A
NM_000093.5:c.315T>A MANE Select NP_000084.3:p.Thr105=