Canonical Allele Identifier: CA351556309

Gene: GRIP2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14506876G>A , CM000665.2:g.14506876G>A	GRCh38
NC_000003.11:g.14548384G>A , CM000665.1:g.14548384G>A	GRCh37
NC_000003.10:g.14523388G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001080423.4:c.2323C>T MANE Select	NP_001073892.3:p.Pro775Ser
ENST00000621039.5:c.2323C>T MANE Select	ENSP00000478352.1:p.Pro775Ser
NM_001080423.3:c.2323C>T	NP_001073892.3:p.Pro775Ser
ENST00000430219.1:c.685C>T	ENSP00000481670.1:p.Pro229Ser
ENST00000430219.2:c.698C>T
ENST00000619221.4:c.2614C>T	ENSP00000480660.1:p.Pro872Ser
ENST00000621039.4:c.2323C>T	ENSP00000478352.1:p.Pro775Ser
ENST00000637182.1:c.2338C>T	ENSP00000490949.1:p.Pro780Ser
XM_011534141.1:c.2344C>T	XP_011532443.1:p.Pro782Ser
XM_011534141.3:c.2344C>T	XP_011532443.1:p.Pro782Ser
XM_011534142.1:c.2338C>T	XP_011532444.1:p.Pro780Ser
XM_011534142.3:c.2338C>T	XP_011532444.1:p.Pro780Ser
XM_011534143.1:c.2218C>T	XP_011532445.1:p.Pro740Ser
XM_011534143.3:c.2218C>T	XP_011532445.1:p.Pro740Ser
XM_011534144.1:c.1936C>T	XP_011532446.1:p.Pro646Ser
XM_011534145.1:c.1660C>T	XP_011532447.1:p.Pro554Ser
XM_011534145.3:c.1660C>T	XP_011532447.1:p.Pro554Ser
XM_011534146.1:c.1582C>T	XP_011532448.1:p.Pro528Ser
XM_011534146.3:c.1582C>T	XP_011532448.1:p.Pro528Ser
XR_940504.1:n.2440C>T
XR_940504.3:n.2440C>T