Canonical Allele Identifier: CA1120084407
Gene: TSNARE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142231472C>A , CM000670.2:g.142231472C>A GRCh38
NC_000008.10:g.143312833C>A , CM000670.1:g.143312833C>A GRCh37
NC_000008.9:g.143310740C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524325.6:c.1447-1893G>T MANE Select ENSP00000428763.2:n.1447-1893G>T
ENST00000307180.4:c.1450-1893G>T ENSP00000303437.4:n.1450-1893G>T
ENST00000520166.5:c.1450-1893G>T ENSP00000427770.2:n.1450-1893G>T
ENST00000524325.5:c.1447-1893G>T ENSP00000428763.2:n.1447-1893G>T
NM_145003.4:c.1447-1893G>T NP_659440.2:n.1447-1893G>T
NM_001363740.2:c.1450-1893G>T NP_001350669.1:n.1450-1893G>T
NM_001366901.1:c.1444-1893G>T NP_001353830.1:n.1444-1893G>T
XM_017013176.1:c.1915-1893G>T XP_016868665.1:n.1915-1893G>T
XR_001746132.1:n.437-85G>T
NM_145003.5:c.1447-1893G>T MANE Select NP_659440.2:n.1447-1893G>T