Canonical Allele Identifier: CA2170812786

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351626_38351629delinsTGTG , CM000677.2:g.38351626_38351629delinsTGTG	GRCh38
NC_000015.9:g.38643827_38643830delinsTGTG , CM000677.1:g.38643827_38643830delinsTGTG	GRCh37
NC_000015.8:g.36431119_36431122delinsTGTG	NCBI36
NG_008980.1:g.103776_103779delinsTGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.1297_1300delinsTGTG MANE Select	ENSP00000299084.4:p.Cys433=
ENST00000299084.8:c.1297_1300delinsTGTG	ENSP00000299084.4:p.Cys433=
NM_152594.2:c.1297_1300delinsTGTG	NP_689807.1:p.Cys433=
XM_005254202.2:c.1333_1336delinsTGTG	XP_005254259.1:p.Cys445=
XM_005254203.3:c.1075_1078delinsTGTG	XP_005254260.1:p.Cys359=
XM_011521288.1:c.1234_1237delinsTGTG	XP_011519590.1:p.Cys412=
XM_011521289.1:c.1234_1237delinsTGTG	XP_011519591.1:p.Cys412=
XM_011521290.1:c.1234_1237delinsTGTG	XP_011519592.1:p.Cys412=
XM_005254202.3:c.1333_1336delinsTGTG	XP_005254259.1:p.Cys445=
XM_011521289.3:c.1234_1237delinsTGTG	XP_011519591.1:p.Cys412=
NM_152594.3:c.1297_1300delinsTGTG MANE Select	NP_689807.1:p.Cys433=