Canonical Allele Identifier: CA1825162344
Gene: TSNARE1 HGNC NCBI

Linked Data

dbSNP Id: rs186835628
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142231484C>G , CM000670.2:g.142231484C>G GRCh38
NC_000008.10:g.143312845C>G , CM000670.1:g.143312845C>G GRCh37
NC_000008.9:g.143310752C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524325.6:c.1447-1905G>C MANE Select ENSP00000428763.2:n.1447-1905G>C
ENST00000307180.4:c.1450-1905G>C ENSP00000303437.4:n.1450-1905G>C
ENST00000520166.5:c.1450-1905G>C ENSP00000427770.2:n.1450-1905G>C
ENST00000524325.5:c.1447-1905G>C ENSP00000428763.2:n.1447-1905G>C
NM_145003.4:c.1447-1905G>C NP_659440.2:n.1447-1905G>C
NM_001363740.2:c.1450-1905G>C NP_001350669.1:n.1450-1905G>C
NM_001366901.1:c.1444-1905G>C NP_001353830.1:n.1444-1905G>C
XM_017013176.1:c.1915-1905G>C XP_016868665.1:n.1915-1905G>C
XR_001746132.1:n.437-97G>C
NM_145003.5:c.1447-1905G>C MANE Select NP_659440.2:n.1447-1905G>C
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