Canonical Allele Identifier: CA2499219768

Gene: COL5A1

Linked Data

• ClinVar Variation Id: 1069626
• ClinVar RCV Id: RCV002242885
• dbSNP Id: rs2132926166

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134835174dup , CM000671.2:g.134835174dup	GRCh38
NC_000009.11:g.137727020dup , CM000671.1:g.137727020dup	GRCh37
NC_000009.10:g.136866841dup	NCBI36
NG_008030.1:g.198369dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371820.4:c.5340dup	ENSP00000360885.4:p.Tyr1781LeufsTer?
ENST00000371817.8:c.5340dup MANE Select	ENSP00000360882.3:p.Tyr1781LeufsTer?
ENST00000371817.7:c.5340dup	ENSP00000360882.3:p.Tyr1781LeufsTer?
ENST00000371820.3:c.598dup
ENST00000618395.4:c.5340dup	ENSP00000481360.1:p.Tyr1781LeufsTer?
NM_000093.4:c.5340dup	NP_000084.3:p.Tyr1781LeufsTer?
NM_001278074.1:c.5340dup	NP_001265003.1:p.Tyr1781LeufsTer?
NR_103451.2:n.71-14962dup
NM_000093.5:c.5340dup MANE Select	NP_000084.3:p.Tyr1781LeufsTer?