Canonical Allele Identifier: CA2170811869

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349559T= , CM000677.2:g.38349559T=	GRCh38
NC_000015.9:g.38641760T= , CM000677.1:g.38641760T=	GRCh37
NC_000015.8:g.36429052T=	NCBI36
NG_008980.1:g.101709T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.684+36T= MANE Select	ENSP00000299084.4:n.684+36T=
ENST00000299084.8:c.684+36T=	ENSP00000299084.4:n.684+36T=
NM_152594.2:c.684+36T=	NP_689807.1:n.684+36T=
XM_005254202.2:c.720+36T=	XP_005254259.1:n.720+36T=
XM_005254203.3:c.462+36T=	XP_005254260.1:n.462+36T=
XM_011521288.1:c.621+36T=	XP_011519590.1:n.621+36T=
XM_011521289.1:c.621+36T=	XP_011519591.1:n.621+36T=
XM_011521290.1:c.621+36T=	XP_011519592.1:n.621+36T=
XM_005254202.3:c.720+36T=	XP_005254259.1:n.720+36T=
XM_011521289.3:c.621+36T=	XP_011519591.1:n.621+36T=
NM_152594.3:c.684+36T= MANE Select	NP_689807.1:n.684+36T=