Canonical Allele Identifier: CA2710293301

Gene: SPRY4

Linked Data

• dbSNP Id: rs2126986253

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.142314279_142314280del , CM000667.2:g.142314279_142314280del	GRCh38
NC_000005.9:g.141693844_141693845del , CM000667.1:g.141693844_141693845del	GRCh37
NC_000005.8:g.141674028_141674029del	NCBI36
NG_034148.1:g.15779_15780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434127.3:c.832_833del MANE Select	ENSP00000399468.2:p.Thr278GlufsTer?
ENST00000643792.1:n.1514_1515del
ENST00000344120.4:c.901_902del	ENSP00000344967.4:p.Thr301GlufsTer?
ENST00000434127.2:c.832_833del	ENSP00000399468.2:p.Thr278GlufsTer?
NM_001127496.1:c.832_833del	NP_001120968.1:p.Thr278GlufsTer?
NM_001293289.1:c.832_833del	NP_001280218.1:p.Thr278GlufsTer?
NM_001293290.1:c.832_833del	NP_001280219.1:p.Thr278GlufsTer?
NM_030964.3:c.901_902del	NP_112226.2:p.Thr301GlufsTer?
XM_011537685.1:c.901_902del	XP_011535987.1:p.Thr301GlufsTer?
XM_011537685.3:c.901_902del	XP_011535987.1:p.Thr301GlufsTer?
XM_017009910.2:c.832_833del	XP_016865399.1:p.Thr278GlufsTer?
NM_001127496.2:c.832_833del	NP_001120968.1:p.Thr278GlufsTer?
NM_001293289.2:c.832_833del	NP_001280218.1:p.Thr278GlufsTer?
NM_001293290.2:c.832_833del	NP_001280219.1:p.Thr278GlufsTer?
NM_030964.4:c.901_902del	NP_112226.2:p.Thr301GlufsTer?
NM_001127496.3:c.832_833del MANE Select	NP_001120968.1:p.Thr278GlufsTer?
NM_001293289.3:c.832_833del	NP_001280218.1:p.Thr278GlufsTer?
NM_001293290.3:c.832_833del	NP_001280219.1:p.Thr278GlufsTer?
NM_030964.5:c.901_902del	NP_112226.2:p.Thr301GlufsTer?