Canonical Allele Identifier: CA343415155

Gene: DDR2

Linked Data

• dbSNP Id: rs2102198289
• MyVariant Identifiers: chr1:g.162745951A>T (hg19) ; chr1:g.162776161A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162776161A>T , CM000663.2:g.162776161A>T	GRCh38
NC_000001.10:g.162745951A>T , CM000663.1:g.162745951A>T	GRCh37
NC_000001.9:g.161012575A>T	NCBI36
NG_016290.1:g.148724A>T
NG_016290.2:g.149949A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367921.8:c.2074A>T MANE Select	ENSP00000356898.3:p.Thr692Ser
ENST00000446985.6:c.2074A>T	ENSP00000400309.2:p.Thr692Ser
ENST00000367921.7:c.2074A>T	ENSP00000356898.3:p.Thr692Ser
ENST00000367922.7:c.2074A>T	ENSP00000356899.2:p.Thr692Ser
NM_001014796.1:c.2074A>T	NP_001014796.1:p.Thr692Ser
NM_006182.2:c.2074A>T	NP_006173.2:p.Thr692Ser
XM_006711344.2:c.2074A>T	XP_006711407.1:p.Thr692Ser
XM_011509586.1:c.2074A>T	XP_011507888.1:p.Thr692Ser
XM_011509587.1:c.2074A>T	XP_011507889.1:p.Thr692Ser
NM_001014796.2:c.2074A>T	NP_001014796.1:p.Thr692Ser
NM_001354982.1:c.2074A>T	NP_001341911.1:p.Thr692Ser
NM_001354983.1:c.2074A>T	NP_001341912.1:p.Thr692Ser
NM_006182.3:c.2074A>T	NP_006173.2:p.Thr692Ser
XM_011509587.2:c.2074A>T	XP_011507889.1:p.Thr692Ser
NM_006182.4:c.2074A>T MANE Select	NP_006173.2:p.Thr692Ser
NM_001014796.3:c.2074A>T	NP_001014796.1:p.Thr692Ser
NM_001354982.2:c.2074A>T	NP_001341911.1:p.Thr692Ser
NM_001354983.2:c.2074A>T	NP_001341912.1:p.Thr692Ser