Canonical Allele Identifier: CA2170812759

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351546C= , CM000677.2:g.38351546C=	GRCh38
NC_000015.9:g.38643747C= , CM000677.1:g.38643747C=	GRCh37
NC_000015.8:g.36431039C=	NCBI36
NG_008980.1:g.103696C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.1217C= MANE Select	ENSP00000299084.4:p.Ala406=
ENST00000299084.8:c.1217C=	ENSP00000299084.4:p.Ala406=
NM_152594.2:c.1217C=	NP_689807.1:p.Ala406=
XM_005254202.2:c.1253C=	XP_005254259.1:p.Ala418=
XM_005254203.3:c.995C=	XP_005254260.1:p.Ala332=
XM_011521288.1:c.1154C=	XP_011519590.1:p.Ala385=
XM_011521289.1:c.1154C=	XP_011519591.1:p.Ala385=
XM_011521290.1:c.1154C=	XP_011519592.1:p.Ala385=
XM_005254202.3:c.1253C=	XP_005254259.1:p.Ala418=
XM_011521289.3:c.1154C=	XP_011519591.1:p.Ala385=
NM_152594.3:c.1217C= MANE Select	NP_689807.1:p.Ala406=