Canonical Allele Identifier: CA467666314

Gene: COL5A1

Linked Data

• MyVariant Identifiers: chr9:g.137713978T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134822132T>G , CM000671.2:g.134822132T>G	GRCh38
NC_000009.11:g.137713978T>G , CM000671.1:g.137713978T>G	GRCh37
NC_000009.10:g.136853799T>G	NCBI36
NG_008030.1:g.185327T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371820.4:c.4590T>G	ENSP00000360885.4:p.Pro1530=
ENST00000371817.8:c.4590T>G MANE Select	ENSP00000360882.3:p.Pro1530=
ENST00000371817.7:c.4590T>G	ENSP00000360882.3:p.Pro1530=
ENST00000618395.4:c.4590T>G	ENSP00000481360.1:p.Pro1530=
NM_000093.4:c.4590T>G	NP_000084.3:p.Pro1530=
NM_001278074.1:c.4590T>G	NP_001265003.1:p.Pro1530=
NR_103451.2:n.71-1923A>C
XR_929712.1:n.4992T>G
XR_929713.1:n.4992T>G
XM_017014266.2:c.4590T>G	XP_016869755.1:p.Pro1530=
XR_001746183.1:n.4988T>G
NM_000093.5:c.4590T>G MANE Select	NP_000084.3:p.Pro1530=