Canonical Allele Identifier: CA351553529

Gene: GRIP2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14496541G>A , CM000665.2:g.14496541G>A	GRCh38
NC_000003.11:g.14538049G>A , CM000665.1:g.14538049G>A	GRCh37
NC_000003.10:g.14513053G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001080423.4:c.2699C>T MANE Select	NP_001073892.3:p.Thr900Ile
ENST00000621039.5:c.2699C>T MANE Select	ENSP00000478352.1:p.Thr900Ile
NM_001080423.3:c.2699C>T	NP_001073892.3:p.Thr900Ile
ENST00000430219.1:c.1343C>T	ENSP00000481670.1:n.1343C>T
ENST00000430219.2:c.1356C>T
ENST00000619221.4:c.2990C>T	ENSP00000480660.1:p.Thr997Ile
ENST00000621039.4:c.2699C>T	ENSP00000478352.1:p.Thr900Ile
ENST00000637182.1:c.2714C>T	ENSP00000490949.1:p.Thr905Ile
XM_011534141.1:c.2720C>T	XP_011532443.1:p.Thr907Ile
XM_011534141.3:c.2720C>T	XP_011532443.1:p.Thr907Ile
XM_011534142.1:c.2714C>T	XP_011532444.1:p.Thr905Ile
XM_011534142.3:c.2714C>T	XP_011532444.1:p.Thr905Ile
XM_011534143.1:c.2594C>T	XP_011532445.1:p.Thr865Ile
XM_011534143.3:c.2594C>T	XP_011532445.1:p.Thr865Ile
XM_011534144.1:c.2312C>T	XP_011532446.1:p.Thr771Ile
XM_011534145.1:c.2036C>T	XP_011532447.1:p.Thr679Ile
XM_011534145.3:c.2036C>T	XP_011532447.1:p.Thr679Ile
XM_011534146.1:c.1958C>T	XP_011532448.1:p.Thr653Ile
XM_011534146.3:c.1958C>T	XP_011532448.1:p.Thr653Ile
XR_940504.1:n.3098C>T
XR_940504.3:n.3098C>T