Canonical Allele Identifier: CA2170812600

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351171A= , CM000677.2:g.38351171A=	GRCh38
NC_000015.9:g.38643372A= , CM000677.1:g.38643372A=	GRCh37
NC_000015.8:g.36430664A=	NCBI36
NG_008980.1:g.103321A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.842A= MANE Select	ENSP00000299084.4:p.Gln281=
ENST00000299084.8:c.842A=	ENSP00000299084.4:p.Gln281=
NM_152594.2:c.842A=	NP_689807.1:p.Gln281=
XM_005254202.2:c.878A=	XP_005254259.1:p.Gln293=
XM_005254203.3:c.620A=	XP_005254260.1:p.Gln207=
XM_011521288.1:c.779A=	XP_011519590.1:p.Gln260=
XM_011521289.1:c.779A=	XP_011519591.1:p.Gln260=
XM_011521290.1:c.779A=	XP_011519592.1:p.Gln260=
XM_005254202.3:c.878A=	XP_005254259.1:p.Gln293=
XM_011521289.3:c.779A=	XP_011519591.1:p.Gln260=
NM_152594.3:c.842A= MANE Select	NP_689807.1:p.Gln281=