Canonical Allele Identifier: CA2170765628

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253030G= , CM000677.2:g.38253030G=	GRCh38
NC_000015.9:g.38545231G= , CM000677.1:g.38545231G=	GRCh37
NC_000015.8:g.36332523G=	NCBI36
NG_008980.1:g.5180G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-156G= MANE Select	ENSP00000299084.4:n.-156G=
ENST00000299084.8:c.-156G=	ENSP00000299084.4:n.-156G=
ENST00000561205.1:n.183G=
NM_152594.2:c.-156G=	NP_689807.1:n.-156G=
XM_005254202.2:c.-156G=	XP_005254259.1:n.-156G=
XM_005254203.3:c.-203G=	XP_005254260.1:n.-203G=
XM_005254202.3:c.-156G=	XP_005254259.1:n.-156G=
XR_001751484.1:n.87+537C=
NM_152594.3:c.-156G= MANE Select	NP_689807.1:n.-156G=