Canonical Allele Identifier: CA3000292082

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50729776dup , CM000678.2:g.50729776dup	GRCh38
NC_000016.9:g.50763687dup , CM000678.1:g.50763687dup	GRCh37
NC_000016.8:g.49321188dup	NCBI36
NG_007508.1:g.37638dup , LRG_177:g.37638dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-42dup	ENSP00000493088.1:n.2382-42dup
ENST00000646677.2:c.*651-42dup	ENSP00000496533.1:n.*651-42dup
ENST00000697428.1:n.2364-42dup
ENST00000641284.1:c.2382-42dup	ENSP00000493088.1:n.2382-42dup
ENST00000646677.1:c.*651-42dup	ENSP00000496533.1:n.*651-42dup
ENST00000647318.2:c.2886-42dup MANE Select	ENSP00000495993.1:n.2886-42dup
ENST00000300589.6:c.2967-42dup	ENSP00000300589.2:n.2967-42dup
NM_001293557.1:c.2886-42dup	NP_001280486.1:n.2886-42dup
NM_022162.2:c.2967-42dup	NP_071445.1:n.2967-42dup
XM_005256084.2:c.2886-42dup	XP_005256141.1:n.2886-42dup
XM_006721242.2:c.2802-42dup	XP_006721305.1:n.2802-42dup
XM_011523257.1:c.2463-42dup	XP_011521559.1:n.2463-42dup
XM_011523258.1:c.2463-42dup	XP_011521560.1:n.2463-42dup
XM_011523259.1:c.2301-42dup	XP_011521561.1:n.2301-42dup
XM_005256084.4:c.2886-42dup	XP_005256141.1:n.2886-42dup
XM_006721242.4:c.2802-42dup	XP_006721305.1:n.2802-42dup
XM_011523259.2:c.2301-42dup	XP_011521561.1:n.2301-42dup
XM_017023535.1:c.2394-42dup	XP_016879024.1:n.2394-42dup
XM_017023536.1:c.2301-42dup	XP_016879025.1:n.2301-42dup
XM_017023537.1:c.2301-42dup	XP_016879026.1:n.2301-42dup
XM_017023538.1:c.2301-42dup	XP_016879027.1:n.2301-42dup
NM_001293557.2:c.2886-42dup	NP_001280486.1:n.2886-42dup
NM_001370466.1:c.2886-42dup MANE Select	NP_001357395.1:n.2886-42dup
NM_022162.3:c.2967-42dup	NP_071445.1:n.2967-42dup
NR_163434.1:n.3098-42dup