Canonical Allele Identifier: CA2170812595

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351164A= , CM000677.2:g.38351164A=	GRCh38
NC_000015.9:g.38643365A= , CM000677.1:g.38643365A=	GRCh37
NC_000015.8:g.36430657A=	NCBI36
NG_008980.1:g.103314A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.835A= MANE Select	ENSP00000299084.4:p.Ser279=
ENST00000299084.8:c.835A=	ENSP00000299084.4:p.Ser279=
NM_152594.2:c.835A=	NP_689807.1:p.Ser279=
XM_005254202.2:c.871A=	XP_005254259.1:p.Ser291=
XM_005254203.3:c.613A=	XP_005254260.1:p.Ser205=
XM_011521288.1:c.772A=	XP_011519590.1:p.Ser258=
XM_011521289.1:c.772A=	XP_011519591.1:p.Ser258=
XM_011521290.1:c.772A=	XP_011519592.1:p.Ser258=
XM_005254202.3:c.871A=	XP_005254259.1:p.Ser291=
XM_011521289.3:c.772A=	XP_011519591.1:p.Ser258=
NM_152594.3:c.835A= MANE Select	NP_689807.1:p.Ser279=