Canonical Allele Identifier: CA15677164

Gene: NCAM1

Linked Data

• dbSNP Id: rs12279261
• gnomAD v2: 11-113106455-A-G
• gnomAD v3: 11-113235733-A-G
• gnomAD v4: 11-113235733-A-G
• MyVariant Identifiers: chr11:g.113106455A>G (hg19) ; chr11:g.113235733A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113235733A>G , CM000673.2:g.113235733A>G	GRCh38
NC_000011.9:g.113106455A>G , CM000673.1:g.113106455A>G	GRCh37
NC_000011.8:g.112611665A>G	NCBI36
NG_032036.1:g.279487A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316851.12:c.1825+569A>G MANE Select	ENSP00000318472.8:n.1825+569A>G
ENST00000316851.11:c.1825+569A>G	ENSP00000318472.8:n.1825+569A>G
ENST00000401611.6:c.1795+569A>G	ENSP00000384055.3:n.1795+569A>G
ENST00000525355.5:n.192+569A>G
ENST00000526322.5:c.431-568A>G	ENSP00000479687.1:n.431-568A>G
ENST00000528590.5:c.304-568A>G
ENST00000530543.5:c.494-568A>G	ENSP00000484481.1:n.494-568A>G
ENST00000531044.5:c.1795+569A>G	ENSP00000484943.1:n.1795+569A>G
ENST00000531817.5:c.326-568A>G	ENSP00000475074.1:n.326-568A>G
ENST00000533073.5:c.323+569A>G
ENST00000611284.4:n.2264+569A>G
ENST00000615112.4:c.1825+569A>G	ENSP00000480797.1:n.1825+569A>G
ENST00000615285.4:c.1903+569A>G	ENSP00000479241.1:n.1903+569A>G
ENST00000618266.4:c.1795+569A>G	ENSP00000477835.1:n.1795+569A>G
ENST00000619839.4:c.1903+569A>G	ENSP00000480132.1:n.1903+569A>G
ENST00000620046.4:c.53-20144A>G	ENSP00000482852.1:n.53-20144A>G
ENST00000621128.4:c.1795+569A>G	ENSP00000481083.1:n.1795+569A>G
ENST00000621518.4:c.1796-568A>G	ENSP00000477808.1:n.1796-568A>G
ENST00000621850.4:c.1796-568A>G	ENSP00000480774.1:n.1796-568A>G
NM_000615.6:c.1795+569A>G	NP_000606.3:n.1795+569A>G
NM_001076682.3:c.1796-568A>G	NP_001070150.1:n.1796-568A>G
NM_001242607.1:c.1903+569A>G	NP_001229536.1:n.1903+569A>G
NM_001242608.1:c.1795+569A>G	NP_001229537.1:n.1795+569A>G
NM_181351.4:c.1825+569A>G	NP_851996.2:n.1825+569A>G
NM_000615.7:c.1795+569A>G	NP_000606.3:n.1795+569A>G
NM_001076682.4:c.1796-568A>G	NP_001070150.1:n.1796-568A>G
NM_001242607.2:c.1903+569A>G	NP_001229536.1:n.1903+569A>G
NM_001242608.2:c.1795+569A>G	NP_001229537.1:n.1795+569A>G
NM_181351.5:c.1825+569A>G MANE Select	NP_851996.2:n.1825+569A>G
NM_001386289.1:c.1825+569A>G	NP_001373218.1:n.1825+569A>G
NM_001386290.1:c.1825+569A>G	NP_001373219.1:n.1825+569A>G
NM_001386291.1:c.1795+569A>G	NP_001373220.1:n.1795+569A>G
NM_001386292.1:c.1795+569A>G	NP_001373221.1:n.1795+569A>G
NM_001400603.1:c.1796-568A>G	NP_001387532.1:n.1796-568A>G
NM_001400604.1:c.1826-568A>G	NP_001387533.1:n.1826-568A>G
NM_001400605.1:c.1796-568A>G	NP_001387534.1:n.1796-568A>G
NM_001400606.1:c.1720+569A>G	NP_001387535.1:n.1720+569A>G
NM_001400607.1:c.1796-568A>G	NP_001387536.1:n.1796-568A>G
NM_001400608.1:c.1826-568A>G	NP_001387537.1:n.1826-568A>G
NM_001400609.1:c.1826-568A>G	NP_001387538.1:n.1826-568A>G
NM_001400610.1:c.1795+569A>G	NP_001387539.1:n.1795+569A>G
NM_001400611.1:c.932-568A>G	NP_001387540.1:n.932-568A>G
NM_001400612.1:c.1904-568A>G	NP_001387541.1:n.1904-568A>G
NM_001400613.1:c.931+569A>G	NP_001387542.1:n.931+569A>G
NM_001400614.1:c.931+569A>G	NP_001387543.1:n.931+569A>G
NM_001400615.1:c.1826-568A>G	NP_001387544.1:n.1826-568A>G
NM_001400616.1:c.1903+569A>G	NP_001387545.1:n.1903+569A>G
NM_001400617.1:c.1795+569A>G	NP_001387546.1:n.1795+569A>G
NM_001400618.1:c.1796-568A>G	NP_001387547.1:n.1796-568A>G
NM_001400619.1:c.931+569A>G	NP_001387548.1:n.931+569A>G
NM_001400620.1:c.1796-568A>G	NP_001387549.1:n.1796-568A>G
NM_001400621.1:c.1826-568A>G	NP_001387550.1:n.1826-568A>G
NM_001400622.1:c.1795+569A>G	NP_001387551.1:n.1795+569A>G
NM_001400623.1:c.1796-568A>G	NP_001387552.1:n.1796-568A>G
NM_001400624.1:c.1825+569A>G	NP_001387553.1:n.1825+569A>G