Canonical Allele Identifier: CA1825162290
Gene: TSNARE1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142231337G= , CM000670.2:g.142231337G= GRCh38
NC_000008.10:g.143312698G= , CM000670.1:g.143312698G= GRCh37
NC_000008.9:g.143310605G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524325.6:c.1447-1758C= MANE Select ENSP00000428763.2:n.1447-1758C=
ENST00000307180.4:c.1450-1758C= ENSP00000303437.4:n.1450-1758C=
ENST00000520166.5:c.1450-1758C= ENSP00000427770.2:n.1450-1758C=
ENST00000524325.5:c.1447-1758C= ENSP00000428763.2:n.1447-1758C=
NM_145003.4:c.1447-1758C= NP_659440.2:n.1447-1758C=
NM_001363740.2:c.1450-1758C= NP_001350669.1:n.1450-1758C=
NM_001366901.1:c.1444-1758C= NP_001353830.1:n.1444-1758C=
XM_017013176.1:c.1915-1758C= XP_016868665.1:n.1915-1758C=
XR_001746132.1:n.487C=
NM_145003.5:c.1447-1758C= MANE Select NP_659440.2:n.1447-1758C=
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