Canonical Allele Identifier: CA2170811814

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349436G= , CM000677.2:g.38349436G=	GRCh38
NC_000015.9:g.38641637G= , CM000677.1:g.38641637G=	GRCh37
NC_000015.8:g.36428929G=	NCBI36
NG_008980.1:g.101586G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.597G= MANE Select	ENSP00000299084.4:p.Gln199=
ENST00000299084.8:c.597G=	ENSP00000299084.4:p.Gln199=
NM_152594.2:c.597G=	NP_689807.1:p.Gln199=
XM_005254202.2:c.633G=	XP_005254259.1:p.Gln211=
XM_005254203.3:c.375G=	XP_005254260.1:p.Gln125=
XM_011521288.1:c.534G=	XP_011519590.1:p.Gln178=
XM_011521289.1:c.534G=	XP_011519591.1:p.Gln178=
XM_011521290.1:c.534G=	XP_011519592.1:p.Gln178=
XM_005254202.3:c.633G=	XP_005254259.1:p.Gln211=
XM_011521289.3:c.534G=	XP_011519591.1:p.Gln178=
NM_152594.3:c.597G= MANE Select	NP_689807.1:p.Gln199=