Canonical Allele Identifier: CA467666762

Gene: COL5A1

Linked Data

• MyVariant Identifiers: chr9:g.137726852T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134835006T>C , CM000671.2:g.134835006T>C	GRCh38
NC_000009.11:g.137726852T>C , CM000671.1:g.137726852T>C	GRCh37
NC_000009.10:g.136866673T>C	NCBI36
NG_008030.1:g.198201T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371820.4:c.5172T>C	ENSP00000360885.4:p.Gly1724=
ENST00000371817.8:c.5172T>C MANE Select	ENSP00000360882.3:p.Gly1724=
ENST00000371817.7:c.5172T>C	ENSP00000360882.3:p.Gly1724=
ENST00000371820.3:c.430T>C
ENST00000618395.4:c.5172T>C	ENSP00000481360.1:p.Gly1724=
NM_000093.4:c.5172T>C	NP_000084.3:p.Gly1724=
NM_001278074.1:c.5172T>C	NP_001265003.1:p.Gly1724=
NR_103451.2:n.71-14797A>G
XR_929712.1:n.5856T>C
XR_929713.1:n.5724T>C
NM_000093.5:c.5172T>C MANE Select	NP_000084.3:p.Gly1724=