Canonical Allele Identifier: CA848637426

Gene: TSNARE1

Linked Data

• dbSNP Id: rs1455904427
• gnomAD v3: 8-142231321-C-A
• gnomAD v4: 8-142231321-C-A
• MyVariant Identifiers: chr8:g.143312682C>A (hg19) ; chr8:g.142231321C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142231321C>A , CM000670.2:g.142231321C>A	GRCh38
NC_000008.10:g.143312682C>A , CM000670.1:g.143312682C>A	GRCh37
NC_000008.9:g.143310589C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524325.6:c.1447-1742G>T MANE Select	ENSP00000428763.2:n.1447-1742G>T
ENST00000307180.4:c.1450-1742G>T	ENSP00000303437.4:n.1450-1742G>T
ENST00000520166.5:c.1450-1742G>T	ENSP00000427770.2:n.1450-1742G>T
ENST00000524325.5:c.1447-1742G>T	ENSP00000428763.2:n.1447-1742G>T
NM_145003.4:c.1447-1742G>T	NP_659440.2:n.1447-1742G>T
NM_001363740.2:c.1450-1742G>T	NP_001350669.1:n.1450-1742G>T
NM_001366901.1:c.1444-1742G>T	NP_001353830.1:n.1444-1742G>T
XM_017013176.1:c.1915-1742G>T	XP_016868665.1:n.1915-1742G>T
XR_001746132.1:n.503G>T
NM_145003.5:c.1447-1742G>T MANE Select	NP_659440.2:n.1447-1742G>T