Canonical Allele Identifier: CA318691588
Gene: NCAM2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.21317024G>A , CM000683.2:g.21317024G>A GRCh38
NC_000021.8:g.22689344G>A , CM000683.1:g.22689344G>A GRCh37
NC_000021.7:g.21611215G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400546.6:c.620-7359G>A MANE Select ENSP00000383392.1:n.620-7359G>A
ENST00000284894.8:c.566-7359G>A ENSP00000284894.8:n.566-7359G>A
ENST00000400546.5:c.620-7359G>A ENSP00000383392.1:n.620-7359G>A
ENST00000461281.1:n.214-7359G>A
NM_004540.3:c.620-7359G>A NP_004531.2:n.620-7359G>A
XM_011529575.1:c.695-7359G>A XP_011527877.1:n.695-7359G>A
XM_011529576.1:c.695-7359G>A XP_011527878.1:n.695-7359G>A
XM_011529577.1:c.695-7359G>A XP_011527879.1:n.695-7359G>A
XM_011529578.1:c.695-7359G>A XP_011527880.1:n.695-7359G>A
XM_011529579.1:c.620-7359G>A XP_011527881.1:n.620-7359G>A
XM_011529580.1:c.695-7359G>A XP_011527882.1:n.695-7359G>A
XM_011529581.1:c.695-7359G>A XP_011527883.1:n.695-7359G>A
XM_011529582.1:c.695-7359G>A XP_011527884.1:n.695-7359G>A
XM_011529583.1:c.146-7359G>A XP_011527885.1:n.146-7359G>A
XM_011529584.1:c.128-7359G>A XP_011527886.1:n.128-7359G>A
XM_011529585.1:c.128-7359G>A XP_011527887.1:n.128-7359G>A
XR_937498.1:n.843-7359G>A
NM_001352591.1:c.620-7359G>A NP_001339520.1:n.620-7359G>A
NM_001352592.1:c.695-7359G>A NP_001339521.1:n.695-7359G>A
NM_001352593.1:c.620-7359G>A NP_001339522.1:n.620-7359G>A
NM_001352594.1:c.620-7359G>A NP_001339523.1:n.620-7359G>A
NM_001352595.1:c.194-7359G>A NP_001339524.1:n.194-7359G>A
NM_001352596.1:c.620-7359G>A NP_001339525.1:n.620-7359G>A
NM_001352597.1:c.695-7359G>A NP_001339526.1:n.695-7359G>A
NM_004540.4:c.620-7359G>A NP_004531.2:n.620-7359G>A
XM_011529575.3:c.695-7359G>A XP_011527877.1:n.695-7359G>A
XM_011529576.3:c.695-7359G>A XP_011527878.1:n.695-7359G>A
XM_011529580.3:c.695-7359G>A XP_011527882.1:n.695-7359G>A
XM_011529581.3:c.695-7359G>A XP_011527883.1:n.695-7359G>A
XM_011529582.3:c.695-7359G>A XP_011527884.1:n.695-7359G>A
XM_011529585.3:c.128-7359G>A XP_011527887.1:n.128-7359G>A
XM_017028356.2:c.128-7359G>A XP_016883845.1:n.128-7359G>A
XM_017028357.2:c.128-7359G>A XP_016883846.1:n.128-7359G>A
XM_024452081.1:c.620-7359G>A XP_024307849.1:n.620-7359G>A
NM_004540.5:c.620-7359G>A MANE Select NP_004531.2:n.620-7359G>A
NM_001352591.2:c.620-7359G>A NP_001339520.1:n.620-7359G>A
NM_001352592.2:c.695-7359G>A NP_001339521.1:n.695-7359G>A
NM_001352593.2:c.620-7359G>A NP_001339522.1:n.620-7359G>A
NM_001352594.2:c.620-7359G>A NP_001339523.1:n.620-7359G>A
NM_001352595.2:c.194-7359G>A NP_001339524.1:n.194-7359G>A
NM_001352596.2:c.620-7359G>A NP_001339525.1:n.620-7359G>A
NM_001352597.2:c.695-7359G>A NP_001339526.1:n.695-7359G>A
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