Canonical Allele Identifier: CA2170812766

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351558T= , CM000677.2:g.38351558T=	GRCh38
NC_000015.9:g.38643759T= , CM000677.1:g.38643759T=	GRCh37
NC_000015.8:g.36431051T=	NCBI36
NG_008980.1:g.103708T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1229T= MANE Select	ENSP00000299084.4:p.Leu410=
ENST00000299084.8:c.1229T=	ENSP00000299084.4:p.Leu410=
NM_152594.2:c.1229T=	NP_689807.1:p.Leu410=
XM_005254202.2:c.1265T=	XP_005254259.1:p.Leu422=
XM_005254203.3:c.1007T=	XP_005254260.1:p.Leu336=
XM_011521288.1:c.1166T=	XP_011519590.1:p.Leu389=
XM_011521289.1:c.1166T=	XP_011519591.1:p.Leu389=
XM_011521290.1:c.1166T=	XP_011519592.1:p.Leu389=
XM_005254202.3:c.1265T=	XP_005254259.1:p.Leu422=
XM_011521289.3:c.1166T=	XP_011519591.1:p.Leu389=
NM_152594.3:c.1229T= MANE Select	NP_689807.1:p.Leu410=