Canonical Allele Identifier: CA2170765653

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253063G= , CM000677.2:g.38253063G=	GRCh38
NC_000015.9:g.38545264G= , CM000677.1:g.38545264G=	GRCh37
NC_000015.8:g.36332556G=	NCBI36
NG_008980.1:g.5213G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.-123G= MANE Select	ENSP00000299084.4:n.-123G=
ENST00000299084.8:c.-123G=	ENSP00000299084.4:n.-123G=
ENST00000561205.1:n.216G=
NM_152594.2:c.-123G=	NP_689807.1:n.-123G=
XM_005254202.2:c.-123G=	XP_005254259.1:n.-123G=
XM_005254203.3:c.-170G=	XP_005254260.1:n.-170G=
XM_005254202.3:c.-123G=	XP_005254259.1:n.-123G=
XR_001751484.1:n.87+504C=
NM_152594.3:c.-123G= MANE Select	NP_689807.1:n.-123G=