Canonical Allele Identifier: CA890314558

Gene: DDR2

Linked Data

• dbSNP Id: rs1458659142
• gnomAD v3: 1-162691149-G-A
• gnomAD v4: 1-162691149-G-A
• MyVariant Identifiers: chr1:g.162660939G>A (hg19) ; chr1:g.162691149G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162691149G>A , CM000663.2:g.162691149G>A	GRCh38
NC_000001.10:g.162660939G>A , CM000663.1:g.162660939G>A	GRCh37
NC_000001.9:g.160927563G>A	NCBI36
NG_016290.1:g.63712G>A
NG_016290.2:g.64937G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367921.8:c.-27-27888G>A MANE Select	ENSP00000356898.3:n.-27-27888G>A
ENST00000446985.6:c.-27-27888G>A	ENSP00000400309.2:n.-27-27888G>A
ENST00000671979.1:c.-107-13903G>A	ENSP00000500822.1:n.-107-13903G>A
ENST00000672207.1:n.360-27888G>A
ENST00000673239.1:n.463+13803G>A
ENST00000367921.7:c.-27-27888G>A	ENSP00000356898.3:n.-27-27888G>A
ENST00000367922.7:c.-107-13903G>A	ENSP00000356899.2:n.-107-13903G>A
ENST00000415555.5:c.-27-27888G>A	ENSP00000391310.1:n.-27-27888G>A
ENST00000446985.5:c.-27-27888G>A	ENSP00000400309.1:n.-27-27888G>A
NM_001014796.1:c.-107-13903G>A	NP_001014796.1:n.-107-13903G>A
NM_006182.2:c.-27-27888G>A	NP_006173.2:n.-27-27888G>A
XM_006711344.2:c.-27-27888G>A	XP_006711407.1:n.-27-27888G>A
XM_011509586.1:c.-27-27888G>A	XP_011507888.1:n.-27-27888G>A
XM_011509587.1:c.-107-13903G>A	XP_011507889.1:n.-107-13903G>A
NM_001014796.2:c.-107-13903G>A	NP_001014796.1:n.-107-13903G>A
NM_001354982.1:c.-27-27888G>A	NP_001341911.1:n.-27-27888G>A
NM_001354983.1:c.-27-27888G>A	NP_001341912.1:n.-27-27888G>A
NM_006182.3:c.-27-27888G>A	NP_006173.2:n.-27-27888G>A
XM_011509587.2:c.-107-13903G>A	XP_011507889.1:n.-107-13903G>A
XM_011509588.3:c.-27-27888G>A	XP_011507890.1:n.-27-27888G>A
NM_006182.4:c.-27-27888G>A MANE Select	NP_006173.2:n.-27-27888G>A
NM_001014796.3:c.-107-13903G>A	NP_001014796.1:n.-107-13903G>A
NM_001354982.2:c.-27-27888G>A	NP_001341911.1:n.-27-27888G>A
NM_001354983.2:c.-27-27888G>A	NP_001341912.1:n.-27-27888G>A