Canonical Allele Identifier: CA2170813039

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352190G= , CM000677.2:g.38352190G=	GRCh38
NC_000015.9:g.38644391G= , CM000677.1:g.38644391G=	GRCh37
NC_000015.8:g.36431683G=	NCBI36
NG_008980.1:g.104340G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.*526G= MANE Select	ENSP00000299084.4:n.*526G=
ENST00000299084.8:c.*526G=	ENSP00000299084.4:n.*526G=
NM_152594.2:c.*526G=	NP_689807.1:n.*526G=
XM_005254202.2:c.*526G=	XP_005254259.1:n.*526G=
XM_005254203.3:c.*526G=	XP_005254260.1:n.*526G=
XM_011521288.1:c.*526G=	XP_011519590.1:n.*526G=
XM_011521289.1:c.*526G=	XP_011519591.1:n.*526G=
XM_011521290.1:c.*526G=	XP_011519592.1:n.*526G=
XM_005254202.3:c.*526G=	XP_005254259.1:n.*526G=
XM_011521289.3:c.*526G=	XP_011519591.1:n.*526G=
NM_152594.3:c.*526G= MANE Select	NP_689807.1:n.*526G=