Canonical Allele Identifier: CA2170765537

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252957G= , CM000677.2:g.38252957G=	GRCh38
NC_000015.9:g.38545158G= , CM000677.1:g.38545158G=	GRCh37
NC_000015.8:g.36332450G=	NCBI36
NG_008980.1:g.5107G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-229G= MANE Select	ENSP00000299084.4:n.-229G=
ENST00000299084.8:c.-229G=	ENSP00000299084.4:n.-229G=
ENST00000561205.1:n.110G=
NM_152594.2:c.-229G=	NP_689807.1:n.-229G=
XM_005254202.2:c.-229G=	XP_005254259.1:n.-229G=
XM_005254203.3:c.-276G=	XP_005254260.1:n.-276G=
XM_005254202.3:c.-229G=	XP_005254259.1:n.-229G=
XR_001751484.1:n.87+610C=
NM_152594.3:c.-229G= MANE Select	NP_689807.1:n.-229G=