Canonical Allele Identifier: CA1825162274

Gene: TSNARE1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142231288_142231290delinsTAA , CM000670.2:g.142231288_142231290delinsTAA	GRCh38
NC_000008.10:g.143312649_143312651delinsTAA , CM000670.1:g.143312649_143312651delinsTAA	GRCh37
NC_000008.9:g.143310556_143310558delinsTAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524325.6:c.1447-1711_1447-1709delinsTTA MANE Select	ENSP00000428763.2:n.1447-1711_1447-1709delinsTTA
ENST00000307180.4:c.1450-1711_1450-1709delinsTTA	ENSP00000303437.4:n.1450-1711_1450-1709delinsTTA
ENST00000520166.5:c.1450-1711_1450-1709delinsTTA	ENSP00000427770.2:n.1450-1711_1450-1709delinsTTA
ENST00000524325.5:c.1447-1711_1447-1709delinsTTA	ENSP00000428763.2:n.1447-1711_1447-1709delinsTTA
NM_145003.4:c.1447-1711_1447-1709delinsTTA	NP_659440.2:n.1447-1711_1447-1709delinsTTA
NM_001363740.2:c.1450-1711_1450-1709delinsTTA	NP_001350669.1:n.1450-1711_1450-1709delinsTTA
NM_001366901.1:c.1444-1711_1444-1709delinsTTA	NP_001353830.1:n.1444-1711_1444-1709delinsTTA
XM_017013176.1:c.1915-1711_1915-1709delinsTTA	XP_016868665.1:n.1915-1711_1915-1709delinsTTA
NM_145003.5:c.1447-1711_1447-1709delinsTTA MANE Select	NP_659440.2:n.1447-1711_1447-1709delinsTTA