Canonical Allele Identifier: CA1825162282

Gene: TSNARE1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142231308_142231310delinsTCA , CM000670.2:g.142231308_142231310delinsTCA	GRCh38
NC_000008.10:g.143312669_143312671delinsTCA , CM000670.1:g.143312669_143312671delinsTCA	GRCh37
NC_000008.9:g.143310576_143310578delinsTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524325.6:c.1447-1731_1447-1729delinsTGA MANE Select	ENSP00000428763.2:n.1447-1731_1447-1729delinsTGA
ENST00000307180.4:c.1450-1731_1450-1729delinsTGA	ENSP00000303437.4:n.1450-1731_1450-1729delinsTGA
ENST00000520166.5:c.1450-1731_1450-1729delinsTGA	ENSP00000427770.2:n.1450-1731_1450-1729delinsTGA
ENST00000524325.5:c.1447-1731_1447-1729delinsTGA	ENSP00000428763.2:n.1447-1731_1447-1729delinsTGA
NM_145003.4:c.1447-1731_1447-1729delinsTGA	NP_659440.2:n.1447-1731_1447-1729delinsTGA
NM_001363740.2:c.1450-1731_1450-1729delinsTGA	NP_001350669.1:n.1450-1731_1450-1729delinsTGA
NM_001366901.1:c.1444-1731_1444-1729delinsTGA	NP_001353830.1:n.1444-1731_1444-1729delinsTGA
XM_017013176.1:c.1915-1731_1915-1729delinsTGA	XP_016868665.1:n.1915-1731_1915-1729delinsTGA
XR_001746132.1:n.514_516delinsTGA
NM_145003.5:c.1447-1731_1447-1729delinsTGA MANE Select	NP_659440.2:n.1447-1731_1447-1729delinsTGA