Canonical Allele Identifier: CA349866819

Gene: COL5A2

Linked Data

• gnomAD v4: 2-189050580-G-A
• MyVariant Identifiers: chr2:g.189915306G>A (hg19) ; chr2:g.189050580G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189050580G>A , CM000664.2:g.189050580G>A	GRCh38
NC_000002.11:g.189915306G>A , CM000664.1:g.189915306G>A	GRCh37
NC_000002.10:g.189623551G>A	NCBI36
NG_011799.1:g.134300C>T
NG_011799.2:g.134300C>T
NG_011799.3:g.179722C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.3028C>T MANE Select	ENSP00000364000.3:p.Pro1010Ser
ENST00000374866.7:c.3028C>T	ENSP00000364000.3:p.Pro1010Ser
ENST00000618828.1:c.1867C>T	ENSP00000482184.1:p.Pro623Ser
NM_000393.3:c.3028C>T	NP_000384.2:p.Pro1010Ser
XM_011510573.1:c.2890C>T	XP_011508875.1:p.Pro964Ser
NM_000393.4:c.3028C>T	NP_000384.2:p.Pro1010Ser
XM_011510573.3:c.2890C>T	XP_011508875.1:p.Pro964Ser
NM_000393.5:c.3028C>T MANE Select	NP_000384.2:p.Pro1010Ser