Canonical Allele Identifier: CA309369109

Gene: NTN5 SEC1P

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48663876C>A , CM000681.2:g.48663876C>A	GRCh38
NC_000019.9:g.49167133C>A , CM000681.1:g.49167133C>A	GRCh37
NC_000019.8:g.53858945C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270235.11:c.971-62G>T (NTN5) MANE Select	ENSP00000270235.4:n.971-62G>T
ENST00000270235.8:c.971-62G>T (NTN5)	ENSP00000270235.3:n.971-62G>T
ENST00000430145.3:n.119+609C>A (SEC1P)
ENST00000474419.5:n.147+609C>A (SEC1P)
ENST00000483163.1:n.77-16149C>A (SEC1P)
ENST00000596844.5:c.14-62G>T (NTN5)	ENSP00000469490.1:n.14-62G>T
ENST00000600468.1:n.1087-62G>T (NTN5)
NM_145807.2:c.971-62G>T (NTN5)	NP_665806.1:n.971-62G>T
NR_004401.2:n.179+609C>A (SEC1P)
XM_011526443.1:c.971-62G>T (NTN5)	XP_011524745.1:n.971-62G>T
XM_011526443.3:c.971-62G>T (NTN5)	XP_011524745.1:n.971-62G>T
XM_017026274.1:c.506-62G>T (NTN5)	XP_016881763.1:n.506-62G>T
NM_145807.3:c.971-62G>T (NTN5)	NP_665806.1:n.971-62G>T
NM_145807.4:c.971-62G>T (NTN5) MANE Select	NP_665806.1:n.971-62G>T