Canonical Allele Identifier: CA467666319

Gene: COL5A1

Linked Data

• MyVariant Identifiers: chr9:g.137713984C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134822138C>A , CM000671.2:g.134822138C>A	GRCh38
NC_000009.11:g.137713984C>A , CM000671.1:g.137713984C>A	GRCh37
NC_000009.10:g.136853805C>A	NCBI36
NG_008030.1:g.185333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371820.4:c.4596C>A	ENSP00000360885.4:p.Pro1532=
ENST00000371817.8:c.4596C>A MANE Select	ENSP00000360882.3:p.Pro1532=
ENST00000371817.7:c.4596C>A	ENSP00000360882.3:p.Pro1532=
ENST00000618395.4:c.4596C>A	ENSP00000481360.1:p.Pro1532=
NM_000093.4:c.4596C>A	NP_000084.3:p.Pro1532=
NM_001278074.1:c.4596C>A	NP_001265003.1:p.Pro1532=
NR_103451.2:n.71-1929G>T
XR_929712.1:n.4998C>A
XR_929713.1:n.4998C>A
XM_017014266.2:c.4596C>A	XP_016869755.1:p.Pro1532=
XR_001746183.1:n.4994C>A
NM_000093.5:c.4596C>A MANE Select	NP_000084.3:p.Pro1532=