Canonical Allele Identifier: CA349862500

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189910547A>C (hg19) ; chr2:g.189045821A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189045821A>C , CM000664.2:g.189045821A>C	GRCh38
NC_000002.11:g.189910547A>C , CM000664.1:g.189910547A>C	GRCh37
NC_000002.10:g.189618792A>C	NCBI36
NG_011799.1:g.139059T>G
NG_011799.2:g.139059T>G
NG_011799.3:g.184481T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.3288T>G MANE Select	ENSP00000364000.3:p.Asp1096Glu
ENST00000374866.7:c.3288T>G	ENSP00000364000.3:p.Asp1096Glu
ENST00000618828.1:c.2127T>G	ENSP00000482184.1:p.Asp709Glu
NM_000393.3:c.3288T>G	NP_000384.2:p.Asp1096Glu
XM_011510573.1:c.3150T>G	XP_011508875.1:p.Asp1050Glu
NM_000393.4:c.3288T>G	NP_000384.2:p.Asp1096Glu
XM_011510573.3:c.3150T>G	XP_011508875.1:p.Asp1050Glu
NM_000393.5:c.3288T>G MANE Select	NP_000384.2:p.Asp1096Glu