Canonical Allele Identifier: CA1687671

Gene: SPRED2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.65344736G>A , CM000664.2:g.65344736G>A	GRCh38
NC_000002.11:g.65571870G>A , CM000664.1:g.65571870G>A	GRCh37
NC_000002.10:g.65425374G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_181784.3:c.187C>T MANE Select	NP_861449.2:p.Arg63Ter
ENST00000356388.9:c.187C>T MANE Select	ENSP00000348753.4:p.Arg63Ter
NM_001128210.1:c.178C>T	NP_001121682.1:p.Arg60Ter
NM_001128210.2:c.178C>T	NP_001121682.1:p.Arg60Ter
NM_181784.2:c.187C>T	NP_861449.2:p.Arg63Ter
ENST00000356388.8:c.187C>T	ENSP00000348753.4:p.Arg63Ter
ENST00000426832.1:c.64C>T	ENSP00000414551.1:p.Arg22Ter
ENST00000427238.1:c.51C>T
ENST00000440972.1:c.187C>T	ENSP00000406481.1:p.Arg63Ter
ENST00000443619.6:c.178C>T	ENSP00000393697.2:p.Arg60Ter
ENST00000452315.5:c.232C>T	ENSP00000390595.1:p.Arg78Ter
ENST00000474228.1:n.324C>T
XM_005264200.3:c.187C>T	XP_005264257.2:p.Arg63Ter
XM_005264200.5:c.187C>T	XP_005264257.2:p.Arg63Ter
XM_005264201.1:c.-236C>T	XP_005264258.1:n.-236C>T
XM_005264202.3:c.187C>T	XP_005264259.1:p.Arg63Ter
XM_005264202.5:c.187C>T	XP_005264259.1:p.Arg63Ter
XM_006711966.1:c.187C>T	XP_006712029.1:p.Arg63Ter