Canonical Allele Identifier: CA848637444
Gene: TSNARE1 HGNC NCBI

Linked Data

dbSNP Id: rs922610481
MyVariant Identifiers: chr8:g.143312777_143312778insG (hg19) chr8:g.142231416_142231417insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142231422dup , CM000670.2:g.142231422dup GRCh38
NC_000008.10:g.143312783dup , CM000670.1:g.143312783dup GRCh37
NC_000008.9:g.143310690dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524325.6:c.1447-1838dup MANE Select ENSP00000428763.2:n.1447-1838dup
ENST00000307180.4:c.1450-1838dup ENSP00000303437.4:n.1450-1838dup
ENST00000520166.5:c.1450-1838dup ENSP00000427770.2:n.1450-1838dup
ENST00000524325.5:c.1447-1838dup ENSP00000428763.2:n.1447-1838dup
NM_145003.4:c.1447-1838dup NP_659440.2:n.1447-1838dup
NM_001363740.2:c.1450-1838dup NP_001350669.1:n.1450-1838dup
NM_001366901.1:c.1444-1838dup NP_001353830.1:n.1444-1838dup
XM_017013176.1:c.1915-1838dup XP_016868665.1:n.1915-1838dup
XR_001746132.1:n.437-30dup
NM_145003.5:c.1447-1838dup MANE Select NP_659440.2:n.1447-1838dup
Search 100 bp 5'
Search 100 bp 3'