Canonical Allele Identifier: CA2170812609

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351194_38351203delinsAAATCAGACT , CM000677.2:g.38351194_38351203delinsAAATCAGACT	GRCh38
NC_000015.9:g.38643395_38643404delinsAAATCAGACT , CM000677.1:g.38643395_38643404delinsAAATCAGACT	GRCh37
NC_000015.8:g.36430687_36430696delinsAAATCAGACT	NCBI36
NG_008980.1:g.103344_103353delinsAAATCAGACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.865_874delinsAAATCAGACT MANE Select	ENSP00000299084.4:p.Lys289=
ENST00000299084.8:c.865_874delinsAAATCAGACT	ENSP00000299084.4:p.Lys289=
NM_152594.2:c.865_874delinsAAATCAGACT	NP_689807.1:p.Lys289=
XM_005254202.2:c.901_910delinsAAATCAGACT	XP_005254259.1:p.Lys301=
XM_005254203.3:c.643_652delinsAAATCAGACT	XP_005254260.1:p.Lys215=
XM_011521288.1:c.802_811delinsAAATCAGACT	XP_011519590.1:p.Lys268=
XM_011521289.1:c.802_811delinsAAATCAGACT	XP_011519591.1:p.Lys268=
XM_011521290.1:c.802_811delinsAAATCAGACT	XP_011519592.1:p.Lys268=
XM_005254202.3:c.901_910delinsAAATCAGACT	XP_005254259.1:p.Lys301=
XM_011521289.3:c.802_811delinsAAATCAGACT	XP_011519591.1:p.Lys268=
NM_152594.3:c.865_874delinsAAATCAGACT MANE Select	NP_689807.1:p.Lys289=