Canonical Allele Identifier: CA2170812676

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351334C= , CM000677.2:g.38351334C=	GRCh38
NC_000015.9:g.38643535C= , CM000677.1:g.38643535C=	GRCh37
NC_000015.8:g.36430827C=	NCBI36
NG_008980.1:g.103484C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1005C= MANE Select	ENSP00000299084.4:p.Cys335=
ENST00000299084.8:c.1005C=	ENSP00000299084.4:p.Cys335=
NM_152594.2:c.1005C=	NP_689807.1:p.Cys335=
XM_005254202.2:c.1041C=	XP_005254259.1:p.Cys347=
XM_005254203.3:c.783C=	XP_005254260.1:p.Cys261=
XM_011521288.1:c.942C=	XP_011519590.1:p.Cys314=
XM_011521289.1:c.942C=	XP_011519591.1:p.Cys314=
XM_011521290.1:c.942C=	XP_011519592.1:p.Cys314=
XM_005254202.3:c.1041C=	XP_005254259.1:p.Cys347=
XM_011521289.3:c.942C=	XP_011519591.1:p.Cys314=
NM_152594.3:c.1005C= MANE Select	NP_689807.1:p.Cys335=