Canonical Allele Identifier: CA421451357

Gene: DDR2

Linked Data

• MyVariant Identifiers: chr1:g.162741830G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162772040G>A , CM000663.2:g.162772040G>A	GRCh38
NC_000001.10:g.162741830G>A , CM000663.1:g.162741830G>A	GRCh37
NC_000001.9:g.161008454G>A	NCBI36
NG_016290.1:g.144603G>A
NG_016290.2:g.145828G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367921.8:c.1521G>A MANE Select	ENSP00000356898.3:p.Val507=
ENST00000446985.6:c.1521G>A	ENSP00000400309.2:p.Val507=
ENST00000367921.7:c.1521G>A	ENSP00000356898.3:p.Val507=
ENST00000367922.7:c.1521G>A	ENSP00000356899.2:p.Val507=
ENST00000433757.1:c.298G>A
NM_001014796.1:c.1521G>A	NP_001014796.1:p.Val507=
NM_006182.2:c.1521G>A	NP_006173.2:p.Val507=
XM_006711344.2:c.1521G>A	XP_006711407.1:p.Val507=
XM_011509586.1:c.1521G>A	XP_011507888.1:p.Val507=
XM_011509587.1:c.1521G>A	XP_011507889.1:p.Val507=
NM_001014796.2:c.1521G>A	NP_001014796.1:p.Val507=
NM_001354982.1:c.1521G>A	NP_001341911.1:p.Val507=
NM_001354983.1:c.1521G>A	NP_001341912.1:p.Val507=
NM_006182.3:c.1521G>A	NP_006173.2:p.Val507=
XM_011509587.2:c.1521G>A	XP_011507889.1:p.Val507=
NM_006182.4:c.1521G>A MANE Select	NP_006173.2:p.Val507=
NM_001014796.3:c.1521G>A	NP_001014796.1:p.Val507=
NM_001354982.2:c.1521G>A	NP_001341911.1:p.Val507=
NM_001354983.2:c.1521G>A	NP_001341912.1:p.Val507=