Canonical Allele Identifier: CA1139657030
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 976336
ClinVar RCV Id: RCV001253604

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51026311_51028334del , CM000664.2:g.51026311_51028334del GRCh38
NC_000002.11:g.51253449_51255472del , CM000664.1:g.51253449_51255472del GRCh37
NC_000002.10:g.51106953_51108976del NCBI36
NG_011878.1:g.9205_11228del

Transcript Alleles

HGVS Amino-acid change
ENST00000401669.7:c.-59_772+1193del
ENST00000637511.1:c.-59_772+1193del
ENST00000401669.6:c.-59_772+1193del
ENST00000404971.5:c.-59_871+62del
ENST00000405472.7:c.-59_772+1193del
ENST00000405581.3:c.-59_772+1193del
ENST00000406316.6:c.-59_772+1193del
ENST00000625672.2:c.-59_772+1193del
ENST00000626899.1:c.-59_772+1193del
ENST00000628515.2:c.-59_772+1193del
NM_001135659.1:c.-59_871+62del
NM_004801.4:c.-59_772+1193del
XM_005264642.2:c.-59_772+1193del
XM_005264643.2:c.-59_772+1193del
XM_006712137.2:c.-59_772+1193del
XM_006712140.2:c.-59_772+1193del
XM_006712141.2:c.-59_772+1193del
XM_011533167.1:c.-59_772+1193del
XM_011533168.1:c.-59_772+1193del
XM_011533169.1:c.-59_772+1193del
XM_011533170.1:c.-59_772+1193del
XM_011533171.1:c.-59_772+1193del
XM_011533172.1:c.-59_772+1193del
XM_011533173.1:c.-59_772+1193del
XM_011533174.1:c.-59_772+1193del
XM_011533175.1:c.-59_772+1193del
XM_011533176.1:c.-59_772+1193del
XM_011533177.1:c.-59_772+1193del
XM_011533178.1:c.-59_772+1193del
XM_011533179.1:c.-59_772+1193del
XM_011533180.1:c.-59_772+1193del
NM_001135659.2:c.-59_871+62del
NM_001330077.1:c.-59_772+1193del
NM_001330078.1:c.-59_772+1193del
NM_001330079.1:c.-59_772+1193del
NM_001330081.1:c.-59_772+1193del
NM_001330082.1:c.-59_772+1193del
NM_001330083.1:c.-59_772+1193del
NM_001330084.1:c.-59_772+1193del
NM_001330085.1:c.-59_772+1193del
NM_001330086.1:c.-59_772+1193del
NM_001330087.1:c.-59_772+1193del
NM_001330088.1:c.-59_772+1193del
NM_001330089.1:c.-59_772+1193del
NM_001330090.1:c.-59_772+1193del
NM_001330093.1:c.-59_772+1193del
NM_001330094.1:c.-59_772+1193del
NM_001330095.1:c.-59_772+1193del
NM_001330096.1:c.-59_772+1193del
NM_004801.5:c.-59_772+1193del
XM_005264642.4:c.-59_772+1193del
XM_006712137.4:c.-59_772+1193del
XM_006712140.4:c.-59_772+1193del
XM_011533167.3:c.-59_772+1193del
XM_011533172.3:c.-59_772+1193del
XM_011533175.3:c.-59_772+1193del
XM_011533177.3:c.-59_772+1193del
XM_011533178.3:c.-59_772+1193del
XM_011533180.3:c.-59_772+1193del
XM_017005303.2:c.-59_772+1193del
XM_017005304.2:c.-59_772+1193del
XM_017005305.2:c.-59_772+1193del
XM_017005306.2:c.-59_772+1193del
XM_017005307.2:c.-59_772+1193del
XM_017005308.2:c.-59_772+1193del
XM_017005309.2:c.-59_772+1193del
XM_017005310.2:c.-59_772+1193del
XM_017005311.2:c.-59_772+1193del
XM_017005314.2:c.-59_772+1193del
XM_017005315.2:c.-59_772+1193del
XM_017005316.2:c.-59_772+1193del
XM_017005318.2:c.-59_772+1193del
XM_017005320.2:c.-59_772+1193del
XM_017005321.2:c.-59_772+1193del
XM_017005322.2:c.-59_772+1193del
XM_017005324.2:c.-59_772+1193del
XM_017005325.2:c.-59_772+1193del
XM_017005326.2:c.-59_772+1193del
XM_017005327.2:c.-59_772+1193del
XM_017005329.2:c.-59_772+1193del
XM_024453244.1:c.-59_772+1193del
XM_024453245.1:c.-59_772+1193del
XM_024453246.1:c.-59_772+1193del
NM_001330078.2:c.-59_772+1193del
NM_001330079.2:c.-59_772+1193del
NM_001330081.2:c.-59_772+1193del
NM_001135659.3:c.-59_871+62del
NM_001330077.2:c.-59_772+1193del
NM_001330082.2:c.-59_772+1193del
NM_001330083.2:c.-59_772+1193del
NM_001330084.2:c.-59_772+1193del
NM_001330085.2:c.-59_772+1193del
NM_001330086.2:c.-59_772+1193del
NM_001330087.2:c.-59_772+1193del
NM_001330088.2:c.-59_772+1193del
NM_001330089.2:c.-59_772+1193del
NM_001330090.2:c.-59_772+1193del
NM_001330093.2:c.-59_772+1193del
NM_001330094.2:c.-59_772+1193del
NM_001330095.2:c.-59_772+1193del
NM_001330096.2:c.-59_772+1193del
NM_004801.6:c.-59_772+1193del