Canonical Allele Identifier: CA1825162289
Gene: TSNARE1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142231332T= , CM000670.2:g.142231332T= GRCh38
NC_000008.10:g.143312693T= , CM000670.1:g.143312693T= GRCh37
NC_000008.9:g.143310600T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524325.6:c.1447-1753A= MANE Select ENSP00000428763.2:n.1447-1753A=
ENST00000307180.4:c.1450-1753A= ENSP00000303437.4:n.1450-1753A=
ENST00000520166.5:c.1450-1753A= ENSP00000427770.2:n.1450-1753A=
ENST00000524325.5:c.1447-1753A= ENSP00000428763.2:n.1447-1753A=
NM_145003.4:c.1447-1753A= NP_659440.2:n.1447-1753A=
NM_001363740.2:c.1450-1753A= NP_001350669.1:n.1450-1753A=
NM_001366901.1:c.1444-1753A= NP_001353830.1:n.1444-1753A=
XM_017013176.1:c.1915-1753A= XP_016868665.1:n.1915-1753A=
XR_001746132.1:n.492A=
NM_145003.5:c.1447-1753A= MANE Select NP_659440.2:n.1447-1753A=
Search 100 bp 5'
Search 100 bp 3'