Canonical Allele Identifier: CA13492476
Gene: NCAM1 HGNC NCBI

Linked Data

dbSNP Id: rs3781878
gnomAD v2: 11-113120212-G-A
gnomAD v3: 11-113249490-G-A
gnomAD v4: 11-113249490-G-A
MyVariant Identifiers: chr11:g.113120212G>A (hg19) chr11:g.113249490G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113249490G>A , CM000673.2:g.113249490G>A GRCh38
NC_000011.9:g.113120212G>A , CM000673.1:g.113120212G>A GRCh37
NC_000011.8:g.112625422G>A NCBI36
NG_032036.1:g.293244G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316851.12:c.1828+3120G>A MANE Select ENSP00000318472.8:n.1828+3120G>A
ENST00000316851.11:c.1828+3120G>A ENSP00000318472.8:n.1828+3120G>A
ENST00000401611.6:c.1796-6387G>A ENSP00000384055.3:n.1796-6387G>A
ENST00000525355.5:n.193-6387G>A
ENST00000525691.5:n.330+3120G>A
ENST00000526322.5:c.536-6387G>A ENSP00000479687.1:n.536-6387G>A
ENST00000528590.5:c.369+3120G>A
ENST00000530543.5:c.509-6387G>A ENSP00000484481.1:n.509-6387G>A
ENST00000531044.5:c.1798+3120G>A ENSP00000484943.1:n.1798+3120G>A
ENST00000531817.5:c.672+3120G>A ENSP00000475074.1:n.672+3120G>A
ENST00000533073.5:c.324-6387G>A
ENST00000534516.2:n.263+3120G>A
ENST00000611284.4:n.2267+3120G>A
ENST00000615112.4:c.1826-6384G>A ENSP00000480797.1:n.1826-6384G>A
ENST00000615285.4:c.1904-6384G>A ENSP00000479241.1:n.1904-6384G>A
ENST00000618266.4:c.1796-6384G>A ENSP00000477835.1:n.1796-6384G>A
ENST00000619839.4:c.1906+3120G>A ENSP00000480132.1:n.1906+3120G>A
ENST00000620046.4:c.53-6387G>A ENSP00000482852.1:n.53-6387G>A
ENST00000621128.4:c.1798+3120G>A ENSP00000481083.1:n.1798+3120G>A
ENST00000621518.4:c.1901-6384G>A ENSP00000477808.1:n.1901-6384G>A
ENST00000621850.4:c.1903+3120G>A ENSP00000480774.1:n.1903+3120G>A
NM_000615.6:c.1798+3120G>A NP_000606.3:n.1798+3120G>A
NM_001076682.3:c.1903+3120G>A NP_001070150.1:n.1903+3120G>A
NM_001242607.1:c.1906+3120G>A NP_001229536.1:n.1906+3120G>A
NM_001242608.1:c.1798+3120G>A NP_001229537.1:n.1798+3120G>A
NM_181351.4:c.1828+3120G>A NP_851996.2:n.1828+3120G>A
NM_000615.7:c.1798+3120G>A NP_000606.3:n.1798+3120G>A
NM_001076682.4:c.1903+3120G>A NP_001070150.1:n.1903+3120G>A
NM_001242607.2:c.1906+3120G>A NP_001229536.1:n.1906+3120G>A
NM_001242608.2:c.1798+3120G>A NP_001229537.1:n.1798+3120G>A
NM_181351.5:c.1828+3120G>A MANE Select NP_851996.2:n.1828+3120G>A
NM_001386289.1:c.1826-6387G>A NP_001373218.1:n.1826-6387G>A
NM_001386290.1:c.1826-6387G>A NP_001373219.1:n.1826-6387G>A
NM_001386291.1:c.1796-6387G>A NP_001373220.1:n.1796-6387G>A
NM_001386292.1:c.1796-6387G>A NP_001373221.1:n.1796-6387G>A
NM_001400603.1:c.1811-6387G>A NP_001387532.1:n.1811-6387G>A
NM_001400604.1:c.1841-6387G>A NP_001387533.1:n.1841-6387G>A
NM_001400605.1:c.1901-6387G>A NP_001387534.1:n.1901-6387G>A
NM_001400606.1:c.1721-6387G>A NP_001387535.1:n.1721-6387G>A
NM_001400607.1:c.1859-6387G>A NP_001387536.1:n.1859-6387G>A
NM_001400608.1:c.1889-6387G>A NP_001387537.1:n.1889-6387G>A
NM_001400609.1:c.1931-6387G>A NP_001387538.1:n.1931-6387G>A
NM_001400610.1:c.1796-6387G>A NP_001387539.1:n.1796-6387G>A
NM_001400611.1:c.1037-6387G>A NP_001387540.1:n.1037-6387G>A
NM_001400612.1:c.2009-6387G>A NP_001387541.1:n.2009-6387G>A
NM_001400613.1:c.932-6387G>A NP_001387542.1:n.932-6387G>A
NM_001400614.1:c.932-6387G>A NP_001387543.1:n.932-6387G>A
NM_001400615.1:c.1841-6387G>A NP_001387544.1:n.1841-6387G>A
NM_001400616.1:c.1904-6387G>A NP_001387545.1:n.1904-6387G>A
NM_001400617.1:c.1796-6387G>A NP_001387546.1:n.1796-6387G>A
NM_001400618.1:c.1811-6387G>A NP_001387547.1:n.1811-6387G>A
NM_001400619.1:c.932-6387G>A NP_001387548.1:n.932-6387G>A
NM_001400620.1:c.1811-6387G>A NP_001387549.1:n.1811-6387G>A
NM_001400621.1:c.1931-6387G>A NP_001387550.1:n.1931-6387G>A
NM_001400622.1:c.1796-6387G>A NP_001387551.1:n.1796-6387G>A
NM_001400623.1:c.1901-6387G>A NP_001387552.1:n.1901-6387G>A
NM_001400624.1:c.1826-6387G>A NP_001387553.1:n.1826-6387G>A
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