Canonical Allele Identifier: CA349862574

Gene: COL5A2

Linked Data

• dbSNP Id: rs1685655643
• MyVariant Identifiers: chr2:g.189910576T>G (hg19) ; chr2:g.189045850T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189045850T>G , CM000664.2:g.189045850T>G	GRCh38
NC_000002.11:g.189910576T>G , CM000664.1:g.189910576T>G	GRCh37
NC_000002.10:g.189618821T>G	NCBI36
NG_011799.1:g.139030A>C
NG_011799.2:g.139030A>C
NG_011799.3:g.184452A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.3259A>C MANE Select	ENSP00000364000.3:p.Thr1087Pro
ENST00000374866.7:c.3259A>C	ENSP00000364000.3:p.Thr1087Pro
ENST00000618828.1:c.2098A>C	ENSP00000482184.1:p.Thr700Pro
NM_000393.3:c.3259A>C	NP_000384.2:p.Thr1087Pro
XM_011510573.1:c.3121A>C	XP_011508875.1:p.Thr1041Pro
NM_000393.4:c.3259A>C	NP_000384.2:p.Thr1087Pro
XM_011510573.3:c.3121A>C	XP_011508875.1:p.Thr1041Pro
NM_000393.5:c.3259A>C MANE Select	NP_000384.2:p.Thr1087Pro