Canonical Allele Identifier: CA13944107
Gene: NRXN3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10151731

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.78739276T>G , CM000676.2:g.78739276T>G GRCh38
NC_000014.7:g.78275372T>G NCBI36
NC_000014.8:g.79205619T>G , CM000676.1:g.79205619T>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000335750.6:c.1327+24137T>G ENSP00000338349.6:p.=
ENST00000554719.5:c.925+24137T>G ENSP00000451648.1:p.=
ENST00000554738.5:c.2038+24137T>G ENSP00000450683.1:p.=
ENST00000556496.2:n.1388+24137T>G
ENST00000634266.1:n.1287+24137T>G
ENST00000634499.1:c.2038+24137T>G ENSP00000488920.1:p.=
ENST00000635466.1:c.2044+24137T>G ENSP00000489551.1:p.=
NM_004796.5:c.925+24137T>G VV NP_004787.2:p.=
NR_073547.1:n.3043+24137T>G
XM_005268218.2:c.2080+24137T>G XP_005268275.1:p.=
XM_006720322.2:c.2068+24137T>G XP_006720385.1:p.=
XM_006720323.2:c.2044+24137T>G XP_006720386.1:p.=
XM_011537363.1:c.2080+24137T>G XP_011535665.1:p.=
XM_011537364.1:c.2080+24137T>G XP_011535666.1:p.=
XM_011537365.1:c.2080+24137T>G XP_011535667.1:p.=
XM_011537366.1:c.2056+24137T>G XP_011535668.1:p.=
XM_011537367.1:c.2080+24137T>G XP_011535669.1:p.=
XM_011537368.1:c.2080+24137T>G XP_011535670.1:p.=
XM_011537369.1:c.2080+24137T>G XP_011535671.1:p.=
XM_011537370.1:c.2056+24137T>G XP_011535672.1:p.=
XM_011537371.1:c.2080+24137T>G XP_011535673.1:p.=
XM_011537372.1:c.2080+24137T>G XP_011535674.1:p.=
XM_011537373.1:c.2080+24137T>G XP_011535675.1:p.=
XM_011537374.1:c.2080+24137T>G XP_011535676.1:p.=
XM_011537375.1:c.2080+24137T>G XP_011535677.1:p.=
XM_011537376.1:c.2080+24137T>G XP_011535678.1:p.=
XM_011537377.1:c.988+24137T>G XP_011535679.1:p.=
XR_943561.1:n.3085+24137T>G
XR_943562.1:n.3085+24137T>G
XR_943563.1:n.3085+24137T>G