Canonical Allele Identifier: CA349862521

Gene: COL5A2

Linked Data

• MyVariant Identifiers: chr2:g.189910557G>C (hg19) ; chr2:g.189045831G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189045831G>C , CM000664.2:g.189045831G>C	GRCh38
NC_000002.11:g.189910557G>C , CM000664.1:g.189910557G>C	GRCh37
NC_000002.10:g.189618802G>C	NCBI36
NG_011799.1:g.139049C>G
NG_011799.2:g.139049C>G
NG_011799.3:g.184471C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.3278C>G MANE Select	ENSP00000364000.3:p.Ala1093Gly
ENST00000374866.7:c.3278C>G	ENSP00000364000.3:p.Ala1093Gly
ENST00000618828.1:c.2117C>G	ENSP00000482184.1:p.Ala706Gly
NM_000393.3:c.3278C>G	NP_000384.2:p.Ala1093Gly
XM_011510573.1:c.3140C>G	XP_011508875.1:p.Ala1047Gly
NM_000393.4:c.3278C>G	NP_000384.2:p.Ala1093Gly
XM_011510573.3:c.3140C>G	XP_011508875.1:p.Ala1047Gly
NM_000393.5:c.3278C>G MANE Select	NP_000384.2:p.Ala1093Gly