Canonical Allele Identifier: CA388459256

Gene: SPRY2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.80337296C>G , CM000675.2:g.80337296C>G	GRCh38
NC_000013.10:g.80911431C>G , CM000675.1:g.80911431C>G	GRCh37
NC_000013.9:g.79809432C>G	NCBI36
NG_050650.1:g.8820G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005842.4:c.410G>C MANE Select	NP_005833.1:p.Gly137Ala
ENST00000377104.4:c.410G>C MANE Select	ENSP00000366308.3:p.Gly137Ala
NM_001318536.1:c.410G>C	NP_001305465.1:p.Gly137Ala
NM_001318537.1:c.410G>C	NP_001305466.1:p.Gly137Ala
NM_001318538.1:c.410G>C	NP_001305467.1:p.Gly137Ala
NM_005842.2:c.410G>C	NP_005833.1:p.Gly137Ala
NM_005842.3:c.410G>C	NP_005833.1:p.Gly137Ala
ENST00000377102.5:c.410G>C	ENSP00000366306.1:p.Gly137Ala
ENST00000377104.3:c.410G>C	ENSP00000366308.3:p.Gly137Ala
ENST00000540649.2:c.410G>C	ENSP00000439027.2:p.Gly137Ala
XM_005266217.1:c.410G>C	XP_005266274.1:p.Gly137Ala
XM_006719753.1:c.410G>C	XP_006719816.1:p.Gly137Ala
XM_011534867.1:c.410G>C	XP_011533169.1:p.Gly137Ala