Canonical Allele Identifier: CA2206693113
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764207_9764218delinsGGGAGCTTGATT , CM000678.2:g.9764207_9764218delinsGGGAGCTTGATT GRCh38
NC_000016.9:g.9858064_9858075delinsGGGAGCTTGATT , CM000678.1:g.9858064_9858075delinsGGGAGCTTGATT GRCh37
NC_000016.8:g.9765565_9765576delinsGGGAGCTTGATT NCBI36
NG_011812.1:g.423537_423548delinsAATCAAGCTCCC
NG_011812.2:g.423537_423548delinsAATCAAGCTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.3326_3337delinsAATCAAGCTCCC MANE Select ENSP00000332549.3:p.Lys1109=
ENST00000535259.6:c.2855_2866delinsAATCAAGCTCCC ENSP00000441572.3:p.Lys952=
ENST00000636273.2:n.2919_2930delinsAATCAAGCTCCC
ENST00000674742.1:c.2855_2866delinsAATCAAGCTCCC ENSP00000502200.1:p.Lys952=
ENST00000675398.1:c.*696_*707delinsAATCAAGCTCCC ENSP00000502752.1:n.*696_*707delinsAATCAAGCTCCC
ENST00000330684.3:c.3326_3337delinsAATCAAGCTCCC ENSP00000332549.3:p.Lys1109=
ENST00000396573.6:c.3326_3337delinsAATCAAGCTCCC ENSP00000379818.2:p.Lys1109=
ENST00000396575.6:c.2915_2926delinsAATCAAGCTCCC ENSP00000379820.3:p.Lys972=
ENST00000461292.3:n.2965_2976delinsAATCAAGCTCCC
ENST00000535259.5:c.2915_2926delinsAATCAAGCTCCC ENSP00000441572.2:p.Lys972=
ENST00000562109.5:c.3326_3337delinsAATCAAGCTCCC ENSP00000454998.1:p.Lys1109=
NM_000833.4:c.3326_3337delinsAATCAAGCTCCC NP_000824.1:p.Lys1109=
NM_001134407.2:c.3326_3337delinsAATCAAGCTCCC NP_001127879.1:p.Lys1109=
NM_001134408.2:c.3326_3337delinsAATCAAGCTCCC NP_001127880.1:p.Lys1109=
XM_011522456.1:c.3167_3178delinsAATCAAGCTCCC XP_011520758.1:p.Lys1056=
XM_011522457.1:c.3068_3079delinsAATCAAGCTCCC XP_011520759.1:p.Lys1023=
XM_011522458.1:c.2855_2866delinsAATCAAGCTCCC XP_011520760.1:p.Lys952=
XM_011522459.1:c.2855_2866delinsAATCAAGCTCCC XP_011520761.1:p.Lys952=
XM_011522460.1:c.2855_2866delinsAATCAAGCTCCC XP_011520762.1:p.Lys952=
XM_011522461.1:c.3326_3337delinsAATCAAGCTCCC XP_011520763.1:p.Lys1109=
XM_011522458.3:c.2855_2866delinsAATCAAGCTCCC XP_011520760.1:p.Lys952=
XM_011522461.3:c.3326_3337delinsAATCAAGCTCCC XP_011520763.1:p.Lys1109=
XM_017023172.1:c.3482_3493delinsAATCAAGCTCCC XP_016878661.1:p.Lys1161=
XM_017023173.1:c.3482_3493delinsAATCAAGCTCCC XP_016878662.1:p.Lys1161=
NM_001134407.3:c.3326_3337delinsAATCAAGCTCCC MANE Select NP_001127879.1:p.Lys1109=
NM_000833.5:c.3326_3337delinsAATCAAGCTCCC NP_000824.1:p.Lys1109=