Canonical Allele Identifier: CA2006335611
Gene: NRGN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124742315T= , CM000673.2:g.124742315T= GRCh38
NC_000011.9:g.124612211T= , CM000673.1:g.124612211T= GRCh37
NC_000011.8:g.124117421T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000284292.11:c.15+2216T= MANE Select ENSP00000284292.5:n.15+2216T=
ENST00000284292.10:c.15+2216T= ENSP00000284292.5:n.15+2216T=
ENST00000412681.2:c.15+2216T= ENSP00000399591.1:n.15+2216T=
NM_001126181.1:c.15+2216T= NP_001119653.1:n.15+2216T=
NM_006176.2:c.15+2216T= NP_006167.1:n.15+2216T=
XR_429013.2:n.2268A=
XR_948129.1:n.1756A=
XR_948130.1:n.1289A=
XR_948131.1:n.2085A=
NM_006176.3:c.15+2216T= MANE Select NP_006167.1:n.15+2216T=
NM_001126181.2:c.15+2216T= NP_001119653.1:n.15+2216T=
Search 100 bp 5'
Search 100 bp 3'