Canonical Allele Identifier: CA2170813120

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352335G= , CM000677.2:g.38352335G=	GRCh38
NC_000015.9:g.38644536G= , CM000677.1:g.38644536G=	GRCh37
NC_000015.8:g.36431828G=	NCBI36
NG_008980.1:g.104485G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*671G= MANE Select	ENSP00000299084.4:n.*671G=
ENST00000299084.8:c.*671G=	ENSP00000299084.4:n.*671G=
NM_152594.2:c.*671G=	NP_689807.1:n.*671G=
XM_005254202.2:c.*671G=	XP_005254259.1:n.*671G=
XM_005254203.3:c.*671G=	XP_005254260.1:n.*671G=
XM_011521288.1:c.*671G=	XP_011519590.1:n.*671G=
XM_011521289.1:c.*671G=	XP_011519591.1:n.*671G=
XM_011521290.1:c.*671G=	XP_011519592.1:n.*671G=
XM_005254202.3:c.*671G=	XP_005254259.1:n.*671G=
XM_011521289.3:c.*671G=	XP_011519591.1:n.*671G=
NM_152594.3:c.*671G= MANE Select	NP_689807.1:n.*671G=