Canonical Allele Identifier: CA1021101911

Gene: NCAM2

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.21537795C>A , CM000683.2:g.21537795C>A	GRCh38
NC_000021.8:g.22910116C>A , CM000683.1:g.22910116C>A	GRCh37
NC_000021.7:g.21831987C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400546.6:c.2403-51C>A MANE Select	ENSP00000383392.1:n.2403-51C>A
ENST00000284894.8:c.2349-51C>A	ENSP00000284894.8:n.2349-51C>A
ENST00000400546.5:c.2403-51C>A	ENSP00000383392.1:n.2403-51C>A
NM_004540.3:c.2403-51C>A	NP_004531.2:n.2403-51C>A
XM_011529575.1:c.2514-51C>A	XP_011527877.1:n.2514-51C>A
XM_011529576.1:c.2514-51C>A	XP_011527878.1:n.2514-51C>A
XM_011529577.1:c.2514-51C>A	XP_011527879.1:n.2514-51C>A
XM_011529578.1:c.2478-51C>A	XP_011527880.1:n.2478-51C>A
XM_011529579.1:c.2439-51C>A	XP_011527881.1:n.2439-51C>A
XM_011529583.1:c.1965-51C>A	XP_011527885.1:n.1965-51C>A
XM_011529584.1:c.1947-51C>A	XP_011527886.1:n.1947-51C>A
XM_011529585.1:c.1947-51C>A	XP_011527887.1:n.1947-51C>A
NM_001352591.1:c.2439-51C>A	NP_001339520.1:n.2439-51C>A
NM_001352592.1:c.2478-51C>A	NP_001339521.1:n.2478-51C>A
NM_001352595.1:c.1977-51C>A	NP_001339524.1:n.1977-51C>A
NM_004540.4:c.2403-51C>A	NP_004531.2:n.2403-51C>A
XM_011529575.3:c.2514-51C>A	XP_011527877.1:n.2514-51C>A
XM_011529576.3:c.2514-51C>A	XP_011527878.1:n.2514-51C>A
XM_011529585.3:c.1947-51C>A	XP_011527887.1:n.1947-51C>A
XM_017028356.2:c.1947-51C>A	XP_016883845.1:n.1947-51C>A
XM_017028357.2:c.1911-51C>A	XP_016883846.1:n.1911-51C>A
NM_004540.5:c.2403-51C>A MANE Select	NP_004531.2:n.2403-51C>A
NM_001352591.2:c.2439-51C>A	NP_001339520.1:n.2439-51C>A
NM_001352592.2:c.2478-51C>A	NP_001339521.1:n.2478-51C>A
NM_001352595.2:c.1977-51C>A	NP_001339524.1:n.1977-51C>A