Canonical Allele Identifier: CA2170788900

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299213_38299214delinsCT , CM000677.2:g.38299213_38299214delinsCT	GRCh38
NC_000015.9:g.38591414_38591415delinsCT , CM000677.1:g.38591414_38591415delinsCT	GRCh37
NC_000015.8:g.36378706_36378707delinsCT	NCBI36
NG_008980.1:g.51363_51364delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-160_33-159delinsCT MANE Select	ENSP00000299084.4:n.33-160_33-159delinsCT
ENST00000299084.8:c.33-160_33-159delinsCT	ENSP00000299084.4:n.33-160_33-159delinsCT
ENST00000561205.1:n.371-160_371-159delinsCT
ENST00000561317.1:c.-31-160_-31-159delinsCT	ENSP00000453680.1:n.-31-160_-31-159delinsCT
NM_152594.2:c.33-160_33-159delinsCT	NP_689807.1:n.33-160_33-159delinsCT
XM_005254202.2:c.69-160_69-159delinsCT	XP_005254259.1:n.69-160_69-159delinsCT
XM_005254203.3:c.-15-23028_-15-23027delinsCT	XP_005254260.1:n.-15-23028_-15-23027delinsCT
XM_011521288.1:c.-31-160_-31-159delinsCT	XP_011519590.1:n.-31-160_-31-159delinsCT
XM_011521289.1:c.-31-160_-31-159delinsCT	XP_011519591.1:n.-31-160_-31-159delinsCT
XM_011521290.1:c.-31-160_-31-159delinsCT	XP_011519592.1:n.-31-160_-31-159delinsCT
XM_005254202.3:c.69-160_69-159delinsCT	XP_005254259.1:n.69-160_69-159delinsCT
XM_011521289.3:c.-31-160_-31-159delinsCT	XP_011519591.1:n.-31-160_-31-159delinsCT
NM_152594.3:c.33-160_33-159delinsCT MANE Select	NP_689807.1:n.33-160_33-159delinsCT