Canonical Allele Identifier: CA421615790

Gene: DDR2

Linked Data

• dbSNP Id: rs2102198408
• MyVariant Identifiers: chr1:g.162745962C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162776172C>G , CM000663.2:g.162776172C>G	GRCh38
NC_000001.10:g.162745962C>G , CM000663.1:g.162745962C>G	GRCh37
NC_000001.9:g.161012586C>G	NCBI36
NG_016290.1:g.148735C>G
NG_016290.2:g.149960C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367921.8:c.2085C>G MANE Select	ENSP00000356898.3:p.Ala695=
ENST00000446985.6:c.2085C>G	ENSP00000400309.2:p.Ala695=
ENST00000367921.7:c.2085C>G	ENSP00000356898.3:p.Ala695=
ENST00000367922.7:c.2085C>G	ENSP00000356899.2:p.Ala695=
NM_001014796.1:c.2085C>G	NP_001014796.1:p.Ala695=
NM_006182.2:c.2085C>G	NP_006173.2:p.Ala695=
XM_006711344.2:c.2085C>G	XP_006711407.1:p.Ala695=
XM_011509586.1:c.2085C>G	XP_011507888.1:p.Ala695=
XM_011509587.1:c.2085C>G	XP_011507889.1:p.Ala695=
NM_001014796.2:c.2085C>G	NP_001014796.1:p.Ala695=
NM_001354982.1:c.2085C>G	NP_001341911.1:p.Ala695=
NM_001354983.1:c.2085C>G	NP_001341912.1:p.Ala695=
NM_006182.3:c.2085C>G	NP_006173.2:p.Ala695=
XM_011509587.2:c.2085C>G	XP_011507889.1:p.Ala695=
NM_006182.4:c.2085C>G MANE Select	NP_006173.2:p.Ala695=
NM_001014796.3:c.2085C>G	NP_001014796.1:p.Ala695=
NM_001354982.2:c.2085C>G	NP_001341911.1:p.Ala695=
NM_001354983.2:c.2085C>G	NP_001341912.1:p.Ala695=