Canonical Allele Identifier: CA343415399

Gene: DDR2

Linked Data

• MyVariant Identifiers: chr1:g.162745993T>G (hg19) ; chr1:g.162776203T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162776203T>G , CM000663.2:g.162776203T>G	GRCh38
NC_000001.10:g.162745993T>G , CM000663.1:g.162745993T>G	GRCh37
NC_000001.9:g.161012617T>G	NCBI36
NG_016290.1:g.148766T>G
NG_016290.2:g.149991T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367921.8:c.2116T>G MANE Select	ENSP00000356898.3:p.Phe706Val
ENST00000446985.6:c.2116T>G	ENSP00000400309.2:p.Phe706Val
ENST00000367921.7:c.2116T>G	ENSP00000356898.3:p.Phe706Val
ENST00000367922.7:c.2116T>G	ENSP00000356899.2:p.Phe706Val
NM_001014796.1:c.2116T>G	NP_001014796.1:p.Phe706Val
NM_006182.2:c.2116T>G	NP_006173.2:p.Phe706Val
XM_006711344.2:c.2116T>G	XP_006711407.1:p.Phe706Val
XM_011509586.1:c.2116T>G	XP_011507888.1:p.Phe706Val
XM_011509587.1:c.2116T>G	XP_011507889.1:p.Phe706Val
NM_001014796.2:c.2116T>G	NP_001014796.1:p.Phe706Val
NM_001354982.1:c.2116T>G	NP_001341911.1:p.Phe706Val
NM_001354983.1:c.2116T>G	NP_001341912.1:p.Phe706Val
NM_006182.3:c.2116T>G	NP_006173.2:p.Phe706Val
XM_011509587.2:c.2116T>G	XP_011507889.1:p.Phe706Val
NM_006182.4:c.2116T>G MANE Select	NP_006173.2:p.Phe706Val
NM_001014796.3:c.2116T>G	NP_001014796.1:p.Phe706Val
NM_001354982.2:c.2116T>G	NP_001341911.1:p.Phe706Val
NM_001354983.2:c.2116T>G	NP_001341912.1:p.Phe706Val