Canonical Allele Identifier: CA2170765546

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252965T= , CM000677.2:g.38252965T=	GRCh38
NC_000015.9:g.38545166T= , CM000677.1:g.38545166T=	GRCh37
NC_000015.8:g.36332458T=	NCBI36
NG_008980.1:g.5115T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-221T= MANE Select	ENSP00000299084.4:n.-221T=
ENST00000299084.8:c.-221T=	ENSP00000299084.4:n.-221T=
ENST00000561205.1:n.118T=
NM_152594.2:c.-221T=	NP_689807.1:n.-221T=
XM_005254202.2:c.-221T=	XP_005254259.1:n.-221T=
XM_005254203.3:c.-268T=	XP_005254260.1:n.-268T=
XM_005254202.3:c.-221T=	XP_005254259.1:n.-221T=
XR_001751484.1:n.87+602A=
NM_152594.3:c.-221T= MANE Select	NP_689807.1:n.-221T=