Canonical Allele Identifier: CA1825162354
Gene: TSNARE1 HGNC NCBI

Linked Data

dbSNP Id: rs1817114479
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142231504C>T , CM000670.2:g.142231504C>T GRCh38
NC_000008.10:g.143312865C>T , CM000670.1:g.143312865C>T GRCh37
NC_000008.9:g.143310772C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524325.6:c.1447-1925G>A MANE Select ENSP00000428763.2:n.1447-1925G>A
ENST00000307180.4:c.1450-1925G>A ENSP00000303437.4:n.1450-1925G>A
ENST00000520166.5:c.1450-1925G>A ENSP00000427770.2:n.1450-1925G>A
ENST00000524325.5:c.1447-1925G>A ENSP00000428763.2:n.1447-1925G>A
NM_145003.4:c.1447-1925G>A NP_659440.2:n.1447-1925G>A
NM_001363740.2:c.1450-1925G>A NP_001350669.1:n.1450-1925G>A
NM_001366901.1:c.1444-1925G>A NP_001353830.1:n.1444-1925G>A
XM_017013176.1:c.1915-1925G>A XP_016868665.1:n.1915-1925G>A
XR_001746132.1:n.437-117G>A
NM_145003.5:c.1447-1925G>A MANE Select NP_659440.2:n.1447-1925G>A
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