Canonical Allele Identifier: CA2545411570
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13615529_13615530insCTTCTTCTAAATA , CM000674.2:g.13615529_13615530insCTTCTTCTAAATA GRCh38
NC_000012.11:g.13768463_13768464insCTTCTTCTAAATA , CM000674.1:g.13768463_13768464insCTTCTTCTAAATA GRCh37
NC_000012.10:g.13659730_13659731insCTTCTTCTAAATA NCBI36
NG_031854.1:g.369559_369560insTATTTAGAAGAAG
NG_031854.2:g.371483_371484insTATTTAGAAGAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.1463_1464insTATTTAGAAGAAG MANE Select ENSP00000477455.1:p.Lys488AsnfsTer3
ENST00000609686.3:c.1463_1464insTATTTAGAAGAAG ENSP00000477455.1:p.Lys488AsnfsTer3
NM_000834.3:c.1463_1464insTATTTAGAAGAAG NP_000825.2:p.Lys488AsnfsTer3
XM_011520628.1:c.1463_1464insTATTTAGAAGAAG XP_011518930.1:p.Lys488AsnfsTer3
XM_011520629.1:c.1463_1464insTATTTAGAAGAAG XP_011518931.1:p.Lys488AsnfsTer3
XM_011520630.1:c.1463_1464insTATTTAGAAGAAG XP_011518932.1:p.Lys488AsnfsTer3
XR_931372.1:n.307+303_307+304insCTTCTTCTAAATA
XR_931373.1:n.447+303_447+304insCTTCTTCTAAATA
XR_931374.1:n.246+303_246+304insCTTCTTCTAAATA
NM_000834.4:c.1463_1464insTATTTAGAAGAAG NP_000825.2:p.Lys488AsnfsTer3
XM_011520628.2:c.1463_1464insTATTTAGAAGAAG XP_011518930.1:p.Lys488AsnfsTer3
XM_011520629.2:c.1463_1464insTATTTAGAAGAAG XP_011518931.1:p.Lys488AsnfsTer3
XM_017019219.2:c.1463_1464insTATTTAGAAGAAG XP_016874708.1:p.Lys488AsnfsTer3
XR_001749013.1:n.728+303_728+304insCTTCTTCTAAATA
XR_931372.2:n.444+303_444+304insCTTCTTCTAAATA
XR_931373.2:n.586+303_586+304insCTTCTTCTAAATA
NM_000834.5:c.1463_1464insTATTTAGAAGAAG MANE Select NP_000825.2:p.Lys488AsnfsTer3