Canonical Allele Identifier: CA2746412619

Gene: DDR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162778536del , CM000663.2:g.162778536del	GRCh38
NC_000001.10:g.162748326del , CM000663.1:g.162748326del	GRCh37
NC_000001.9:g.161014950del	NCBI36
NG_016290.1:g.151099del
NG_016290.2:g.152324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367921.8:c.2284-44del MANE Select	ENSP00000356898.3:n.2284-44del
ENST00000446985.6:c.2284-44del	ENSP00000400309.2:n.2284-44del
ENST00000367921.7:c.2284-44del	ENSP00000356898.3:n.2284-44del
ENST00000367922.7:c.2284-44del	ENSP00000356899.2:n.2284-44del
NM_001014796.1:c.2284-44del	NP_001014796.1:n.2284-44del
NM_006182.2:c.2284-44del	NP_006173.2:n.2284-44del
XM_006711344.2:c.2284-44del	XP_006711407.1:n.2284-44del
XM_011509586.1:c.2284-44del	XP_011507888.1:n.2284-44del
XM_011509587.1:c.2284-44del	XP_011507889.1:n.2284-44del
NM_001014796.2:c.2284-44del	NP_001014796.1:n.2284-44del
NM_001354982.1:c.2284-44del	NP_001341911.1:n.2284-44del
NM_001354983.1:c.2284-44del	NP_001341912.1:n.2284-44del
NM_006182.3:c.2284-44del	NP_006173.2:n.2284-44del
XM_011509587.2:c.2284-44del	XP_011507889.1:n.2284-44del
NM_006182.4:c.2284-44del MANE Select	NP_006173.2:n.2284-44del
NM_001014796.3:c.2284-44del	NP_001014796.1:n.2284-44del
NM_001354982.2:c.2284-44del	NP_001341911.1:n.2284-44del
NM_001354983.2:c.2284-44del	NP_001341912.1:n.2284-44del