LDH info

Canonical Allele Identifier: CA264212847
Gene: NRXN3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10083466

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.79518375C>A , CM000676.2:g.79518375C>A GRCh38
NC_000014.8:g.79984718C>A , CM000676.1:g.79984718C>A GRCh37
NC_000014.7:g.79054471C>A NCBI36
NG_052991.1:g.1353003C>A

Transcript Alleles

HGVS Amino-acid change
NM_001105250.2:c.429+50973C>A VV NP_001098720.1:p.=
NM_001272020.1:c.429+50973C>A VV NP_001258949.1:p.=
NM_004796.5:c.2325+50973C>A VV NP_004787.2:p.=
NM_138970.4:c.429+50973C>A VV NP_620426.2:p.=
NR_073546.1:n.1382+50973C>A
NR_073547.1:n.4416+50973C>A
XM_005268218.2:c.3480+50973C>A XP_005268275.1:p.=
XM_006720322.2:c.3468+50973C>A XP_006720385.1:p.=
XM_006720323.2:c.3444+50973C>A XP_006720386.1:p.=
XM_011537363.1:c.3480+50973C>A XP_011535665.1:p.=
XM_011537364.1:c.3480+50973C>A XP_011535666.1:p.=
XM_011537365.1:c.3480+50973C>A XP_011535667.1:p.=
XM_011537366.1:c.3456+50973C>A XP_011535668.1:p.=
XM_011537367.1:c.3480+50973C>A XP_011535669.1:p.=
XM_011537368.1:c.3480+50973C>A XP_011535670.1:p.=
XM_011537369.1:c.3480+50973C>A XP_011535671.1:p.=
XM_011537370.1:c.3456+50973C>A XP_011535672.1:p.=
XM_011537371.1:c.3480+50973C>A XP_011535673.1:p.=
XM_011537372.1:c.3480+50973C>A XP_011535674.1:p.=
XM_011537373.1:c.3480+50973C>A XP_011535675.1:p.=
XM_011537374.1:c.3480+50973C>A XP_011535676.1:p.=
XM_011537375.1:c.3480+50973C>A XP_011535677.1:p.=
XM_011537376.1:c.3480+50973C>A XP_011535678.1:p.=
XM_011537377.1:c.2388+50973C>A XP_011535679.1:p.=
XR_943561.1:n.4485+50973C>A
XR_943562.1:n.4485+50973C>A
XR_943563.1:n.4485+50973C>A
NM_001330195.1:c.3444+50973C>A VV NP_001317124.1:p.=
NM_001366425.1:c.3444+50973C>A VV NP_001353354.1:p.=
NM_001366426.1:c.3456+50973C>A VV NP_001353355.1:p.=
NR_158973.1:n.4461+50973C>A
NR_158974.1:n.4449+50973C>A
NR_158975.1:n.4461+50973C>A
XM_005268218.3:c.3480+50973C>A XP_005268275.1:p.=
XM_011537364.2:c.3480+50973C>A XP_011535666.1:p.=
XM_011537365.2:c.3480+50973C>A XP_011535667.1:p.=
XM_017021790.1:c.3480+50973C>A XP_016877279.1:p.=
XM_017021791.1:c.3480+50973C>A XP_016877280.1:p.=
XM_017021792.1:c.3468+50973C>A XP_016877281.1:p.=
XM_017021793.1:c.3453+50973C>A XP_016877282.1:p.=
XM_017021794.1:c.3444+50973C>A XP_016877283.1:p.=
XM_017021796.2:c.3429+50973C>A XP_016877285.1:p.=
XM_017021797.1:c.3420+50973C>A XP_016877286.1:p.=
XM_017021798.1:c.3417+50973C>A XP_016877287.1:p.=
XM_017021799.2:c.3480+50973C>A XP_016877288.1:p.=
XM_017021800.1:c.3480+50973C>A XP_016877289.1:p.=
XM_017021801.1:c.3453+50973C>A XP_016877290.1:p.=
XM_017021804.1:c.3453+50973C>A XP_016877293.1:p.=
XM_017021805.1:c.3444+50973C>A XP_016877294.1:p.=
XM_017021807.1:c.3480+50973C>A XP_016877296.1:p.=
XM_024449750.1:c.3453+50973C>A XP_024305518.1:p.=
XM_024449751.1:c.3417+50973C>A XP_024305519.1:p.=
XM_024449752.1:c.3468+50973C>A XP_024305520.1:p.=
XM_024449753.1:c.3417+50973C>A XP_024305521.1:p.=
XR_001750599.1:n.4485+50973C>A
XR_001750600.1:n.4485+50973C>A
XR_001750602.1:n.4458+50973C>A
XR_001750604.1:n.4434+50973C>A
XR_001750605.1:n.4434+50973C>A
XR_001750606.1:n.4485+50973C>A
XR_001750607.1:n.4485+50973C>A
XR_001750609.1:n.4485+50973C>A
XR_001750610.1:n.4485+50973C>A
XR_002957572.1:n.4485+50973C>A
XR_943563.2:n.4485+50973C>A
ENST00000281127.11:c.429+50973C>A ENSP00000281127.7:p.=
ENST00000428277.6:c.429+50973C>A ENSP00000394426.2:p.=
ENST00000553803.5:n.296+50973C>A
ENST00000554719.5:c.2325+50973C>A ENSP00000451648.1:p.=
ENST00000554738.5:c.3411+50973C>A ENSP00000450683.1:p.=
ENST00000555073.5:n.395+50973C>A
ENST00000555387.1:c.429+50973C>A ENSP00000451393.1:p.=
ENST00000556003.1:n.281+50973C>A
ENST00000557594.5:c.429+50973C>A ENSP00000451672.1:p.=
ENST00000634499.1:c.3411+50973C>A ENSP00000488920.1:p.=
ENST00000635466.1:c.3444+50973C>A ENSP00000489551.1:p.=