Canonical Allele Identifier: CA14663624

Gene: NTN5 SEC1P

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48664925T>C , CM000681.2:g.48664925T>C	GRCh38
NC_000019.9:g.49168182T>C , CM000681.1:g.49168182T>C	GRCh37
NC_000019.8:g.53859994T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270235.11:c.632-158A>G (NTN5) MANE Select	ENSP00000270235.4:n.632-158A>G
ENST00000270235.8:c.632-158A>G (NTN5)	ENSP00000270235.3:n.632-158A>G
ENST00000430145.3:n.119+1658T>C (SEC1P)
ENST00000474419.5:n.147+1658T>C (SEC1P)
ENST00000483163.1:n.77-15100T>C (SEC1P)
ENST00000596844.5:c.-326-158A>G (NTN5)	ENSP00000469490.1:n.-326-158A>G
ENST00000600468.1:n.748-158A>G (NTN5)
NM_145807.2:c.632-158A>G (NTN5)	NP_665806.1:n.632-158A>G
NR_004401.2:n.179+1658T>C (SEC1P)
XM_011526443.1:c.632-158A>G (NTN5)	XP_011524745.1:n.632-158A>G
XM_011526443.3:c.632-158A>G (NTN5)	XP_011524745.1:n.632-158A>G
XM_017026274.1:c.167-158A>G (NTN5)	XP_016881763.1:n.167-158A>G
NM_145807.3:c.632-158A>G (NTN5)	NP_665806.1:n.632-158A>G
NM_145807.4:c.632-158A>G (NTN5) MANE Select	NP_665806.1:n.632-158A>G