Canonical Allele Identifier: CA2170812764

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351554G= , CM000677.2:g.38351554G=	GRCh38
NC_000015.9:g.38643755G= , CM000677.1:g.38643755G=	GRCh37
NC_000015.8:g.36431047G=	NCBI36
NG_008980.1:g.103704G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1225G= MANE Select	ENSP00000299084.4:p.Ala409=
ENST00000299084.8:c.1225G=	ENSP00000299084.4:p.Ala409=
NM_152594.2:c.1225G=	NP_689807.1:p.Ala409=
XM_005254202.2:c.1261G=	XP_005254259.1:p.Ala421=
XM_005254203.3:c.1003G=	XP_005254260.1:p.Ala335=
XM_011521288.1:c.1162G=	XP_011519590.1:p.Ala388=
XM_011521289.1:c.1162G=	XP_011519591.1:p.Ala388=
XM_011521290.1:c.1162G=	XP_011519592.1:p.Ala388=
XM_005254202.3:c.1261G=	XP_005254259.1:p.Ala421=
XM_011521289.3:c.1162G=	XP_011519591.1:p.Ala388=
NM_152594.3:c.1225G= MANE Select	NP_689807.1:p.Ala409=