Canonical Allele Identifier: CA1203285441
Gene: DDR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162776238A= , CM000663.2:g.162776238A= GRCh38
NC_000001.10:g.162746028A= , CM000663.1:g.162746028A= GRCh37
NC_000001.9:g.161012652A= NCBI36
NG_016290.1:g.148801A=
NG_016290.2:g.150026A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367921.8:c.2151A= MANE Select ENSP00000356898.3:p.Leu717=
ENST00000446985.6:c.2151A= ENSP00000400309.2:p.Leu717=
ENST00000367921.7:c.2151A= ENSP00000356898.3:p.Leu717=
ENST00000367922.7:c.2151A= ENSP00000356899.2:p.Leu717=
NM_001014796.1:c.2151A= NP_001014796.1:p.Leu717=
NM_006182.2:c.2151A= NP_006173.2:p.Leu717=
XM_006711344.2:c.2151A= XP_006711407.1:p.Leu717=
XM_011509586.1:c.2151A= XP_011507888.1:p.Leu717=
XM_011509587.1:c.2151A= XP_011507889.1:p.Leu717=
NM_001014796.2:c.2151A= NP_001014796.1:p.Leu717=
NM_001354982.1:c.2151A= NP_001341911.1:p.Leu717=
NM_001354983.1:c.2151A= NP_001341912.1:p.Leu717=
NM_006182.3:c.2151A= NP_006173.2:p.Leu717=
XM_011509587.2:c.2151A= XP_011507889.1:p.Leu717=
NM_006182.4:c.2151A= MANE Select NP_006173.2:p.Leu717=
NM_001014796.3:c.2151A= NP_001014796.1:p.Leu717=
NM_001354982.2:c.2151A= NP_001341911.1:p.Leu717=
NM_001354983.2:c.2151A= NP_001341912.1:p.Leu717=