Canonical Allele Identifier: CA318666400

Gene: NCAM2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.21115536A>T , CM000683.2:g.21115536A>T	GRCh38
NC_000021.8:g.22487854A>T , CM000683.1:g.22487854A>T	GRCh37
NC_000021.7:g.21409725A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400546.6:c.55+116918A>T MANE Select	ENSP00000383392.1:n.55+116918A>T
ENST00000400546.5:c.55+116918A>T	ENSP00000383392.1:n.55+116918A>T
NM_004540.3:c.55+116918A>T	NP_004531.2:n.55+116918A>T
XM_011529576.1:c.-21-95005A>T	XP_011527878.1:n.-21-95005A>T
XM_011529579.1:c.55+116918A>T	XP_011527881.1:n.55+116918A>T
NM_001352591.1:c.55+116918A>T	NP_001339520.1:n.55+116918A>T
NM_001352592.1:c.-21-95005A>T	NP_001339521.1:n.-21-95005A>T
NM_001352593.1:c.55+116918A>T	NP_001339522.1:n.55+116918A>T
NM_001352594.1:c.55+116918A>T	NP_001339523.1:n.55+116918A>T
NM_001352595.1:c.55+116918A>T	NP_001339524.1:n.55+116918A>T
NM_001352596.1:c.55+116918A>T	NP_001339525.1:n.55+116918A>T
NM_004540.4:c.55+116918A>T	NP_004531.2:n.55+116918A>T
XM_011529576.3:c.-21-95005A>T	XP_011527878.1:n.-21-95005A>T
XM_017028356.2:c.-450+116918A>T	XP_016883845.1:n.-450+116918A>T
XM_017028357.2:c.-450+116918A>T	XP_016883846.1:n.-450+116918A>T
XM_024452081.1:c.55+116918A>T	XP_024307849.1:n.55+116918A>T
NM_004540.5:c.55+116918A>T MANE Select	NP_004531.2:n.55+116918A>T
NM_001352591.2:c.55+116918A>T	NP_001339520.1:n.55+116918A>T
NM_001352592.2:c.-21-95005A>T	NP_001339521.1:n.-21-95005A>T
NM_001352593.2:c.55+116918A>T	NP_001339522.1:n.55+116918A>T
NM_001352594.2:c.55+116918A>T	NP_001339523.1:n.55+116918A>T
NM_001352595.2:c.55+116918A>T	NP_001339524.1:n.55+116918A>T
NM_001352596.2:c.55+116918A>T	NP_001339525.1:n.55+116918A>T