Canonical Allele Identifier: CA2170788909

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299238A= , CM000677.2:g.38299238A=	GRCh38
NC_000015.9:g.38591439A= , CM000677.1:g.38591439A=	GRCh37
NC_000015.8:g.36378731A=	NCBI36
NG_008980.1:g.51388A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-135A= MANE Select	ENSP00000299084.4:n.33-135A=
ENST00000299084.8:c.33-135A=	ENSP00000299084.4:n.33-135A=
ENST00000561205.1:n.371-135A=
ENST00000561317.1:c.-31-135A=	ENSP00000453680.1:n.-31-135A=
NM_152594.2:c.33-135A=	NP_689807.1:n.33-135A=
XM_005254202.2:c.69-135A=	XP_005254259.1:n.69-135A=
XM_005254203.3:c.-15-23003A=	XP_005254260.1:n.-15-23003A=
XM_011521288.1:c.-31-135A=	XP_011519590.1:n.-31-135A=
XM_011521289.1:c.-31-135A=	XP_011519591.1:n.-31-135A=
XM_011521290.1:c.-31-135A=	XP_011519592.1:n.-31-135A=
XM_005254202.3:c.69-135A=	XP_005254259.1:n.69-135A=
XM_011521289.3:c.-31-135A=	XP_011519591.1:n.-31-135A=
NM_152594.3:c.33-135A= MANE Select	NP_689807.1:n.33-135A=