Canonical Allele Identifier: CA591110596

Gene: COL5A1

Linked Data

• dbSNP Id: rs1172418833
• gnomAD v2: 9-137710403-C-G
• gnomAD v3: 9-134818557-C-G
• gnomAD v4: 9-134818557-C-G
• MyVariant Identifiers: chr9:g.137710403C>G (hg19) ; chr9:g.134818557C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134818557C>G , CM000671.2:g.134818557C>G	GRCh38
NC_000009.11:g.137710403C>G , CM000671.1:g.137710403C>G	GRCh37
NC_000009.10:g.136850224C>G	NCBI36
NG_008030.1:g.181752C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371820.4:c.4231-99C>G	ENSP00000360885.4:n.4231-99C>G
ENST00000371817.8:c.4231-99C>G MANE Select	ENSP00000360882.3:n.4231-99C>G
ENST00000371817.7:c.4231-99C>G	ENSP00000360882.3:n.4231-99C>G
ENST00000618395.4:c.4231-99C>G	ENSP00000481360.1:n.4231-99C>G
NM_000093.4:c.4231-99C>G	NP_000084.3:n.4231-99C>G
NM_001278074.1:c.4231-99C>G	NP_001265003.1:n.4231-99C>G
XR_929712.1:n.4633-99C>G
XR_929713.1:n.4633-99C>G
XM_017014266.2:c.4231-99C>G	XP_016869755.1:n.4231-99C>G
XR_001746183.1:n.4629-99C>G
NM_000093.5:c.4231-99C>G MANE Select	NP_000084.3:n.4231-99C>G