Canonical Allele Identifier: CA2170812636

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351255T= , CM000677.2:g.38351255T=	GRCh38
NC_000015.9:g.38643456T= , CM000677.1:g.38643456T=	GRCh37
NC_000015.8:g.36430748T=	NCBI36
NG_008980.1:g.103405T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.926T= MANE Select	ENSP00000299084.4:p.Val309=
ENST00000299084.8:c.926T=	ENSP00000299084.4:p.Val309=
NM_152594.2:c.926T=	NP_689807.1:p.Val309=
XM_005254202.2:c.962T=	XP_005254259.1:p.Val321=
XM_005254203.3:c.704T=	XP_005254260.1:p.Val235=
XM_011521288.1:c.863T=	XP_011519590.1:p.Val288=
XM_011521289.1:c.863T=	XP_011519591.1:p.Val288=
XM_011521290.1:c.863T=	XP_011519592.1:p.Val288=
XM_005254202.3:c.962T=	XP_005254259.1:p.Val321=
XM_011521289.3:c.863T=	XP_011519591.1:p.Val288=
NM_152594.3:c.926T= MANE Select	NP_689807.1:p.Val309=