Canonical Allele Identifier: CA2017462768

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615054_13615057delinsCCTT , CM000674.2:g.13615054_13615057delinsCCTT	GRCh38
NC_000012.11:g.13767988_13767991delinsCCTT , CM000674.1:g.13767988_13767991delinsCCTT	GRCh37
NC_000012.10:g.13659255_13659258delinsCCTT	NCBI36
NG_031854.1:g.370032_370035delinsAAGG
NG_031854.2:g.371956_371959delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+57_1654+60delinsAAGG MANE Select	ENSP00000477455.1:n.1654+57_1654+60delinsAAGG
ENST00000609686.3:c.1654+57_1654+60delinsAAGG	ENSP00000477455.1:n.1654+57_1654+60delinsAAGG
NM_000834.3:c.1654+57_1654+60delinsAAGG	NP_000825.2:n.1654+57_1654+60delinsAAGG
XM_011520628.1:c.1654+57_1654+60delinsAAGG	XP_011518930.1:n.1654+57_1654+60delinsAAGG
XM_011520629.1:c.1654+57_1654+60delinsAAGG	XP_011518931.1:n.1654+57_1654+60delinsAAGG
XM_011520630.1:c.1654+57_1654+60delinsAAGG	XP_011518932.1:n.1654+57_1654+60delinsAAGG
XR_931372.1:n.179-44_179-41delinsCCTT
XR_931373.1:n.319-44_319-41delinsCCTT
XR_931374.1:n.118-44_118-41delinsCCTT
NM_000834.4:c.1654+57_1654+60delinsAAGG	NP_000825.2:n.1654+57_1654+60delinsAAGG
XM_011520628.2:c.1654+57_1654+60delinsAAGG	XP_011518930.1:n.1654+57_1654+60delinsAAGG
XM_011520629.2:c.1654+57_1654+60delinsAAGG	XP_011518931.1:n.1654+57_1654+60delinsAAGG
XM_017019219.2:c.1654+57_1654+60delinsAAGG	XP_016874708.1:n.1654+57_1654+60delinsAAGG
XR_001749013.1:n.600-44_600-41delinsCCTT
XR_931372.2:n.316-44_316-41delinsCCTT
XR_931373.2:n.458-44_458-41delinsCCTT
NM_000834.5:c.1654+57_1654+60delinsAAGG MANE Select	NP_000825.2:n.1654+57_1654+60delinsAAGG