Canonical Allele Identifier: CA2017463243

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615451_13615452delinsTA , CM000674.2:g.13615451_13615452delinsTA	GRCh38
NC_000012.11:g.13768385_13768386delinsTA , CM000674.1:g.13768385_13768386delinsTA	GRCh37
NC_000012.10:g.13659652_13659653delinsTA	NCBI36
NG_031854.1:g.369637_369638delinsTA
NG_031854.2:g.371561_371562delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1500+41_1500+42delinsTA MANE Select	ENSP00000477455.1:n.1500+41_1500+42delinsTA
ENST00000609686.3:c.1500+41_1500+42delinsTA	ENSP00000477455.1:n.1500+41_1500+42delinsTA
NM_000834.3:c.1500+41_1500+42delinsTA	NP_000825.2:n.1500+41_1500+42delinsTA
XM_011520628.1:c.1500+41_1500+42delinsTA	XP_011518930.1:n.1500+41_1500+42delinsTA
XM_011520629.1:c.1500+41_1500+42delinsTA	XP_011518931.1:n.1500+41_1500+42delinsTA
XM_011520630.1:c.1500+41_1500+42delinsTA	XP_011518932.1:n.1500+41_1500+42delinsTA
XR_931372.1:n.307+225_307+226delinsTA
XR_931373.1:n.447+225_447+226delinsTA
XR_931374.1:n.246+225_246+226delinsTA
NM_000834.4:c.1500+41_1500+42delinsTA	NP_000825.2:n.1500+41_1500+42delinsTA
XM_011520628.2:c.1500+41_1500+42delinsTA	XP_011518930.1:n.1500+41_1500+42delinsTA
XM_011520629.2:c.1500+41_1500+42delinsTA	XP_011518931.1:n.1500+41_1500+42delinsTA
XM_017019219.2:c.1500+41_1500+42delinsTA	XP_016874708.1:n.1500+41_1500+42delinsTA
XR_001749013.1:n.728+225_728+226delinsTA
XR_931372.2:n.444+225_444+226delinsTA
XR_931373.2:n.586+225_586+226delinsTA
NM_000834.5:c.1500+41_1500+42delinsTA MANE Select	NP_000825.2:n.1500+41_1500+42delinsTA