Canonical Allele Identifier: CA2170788905

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299224_38299227delinsGCTA , CM000677.2:g.38299224_38299227delinsGCTA	GRCh38
NC_000015.9:g.38591425_38591428delinsGCTA , CM000677.1:g.38591425_38591428delinsGCTA	GRCh37
NC_000015.8:g.36378717_36378720delinsGCTA	NCBI36
NG_008980.1:g.51374_51377delinsGCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-149_33-146delinsGCTA MANE Select	ENSP00000299084.4:n.33-149_33-146delinsGCTA
ENST00000299084.8:c.33-149_33-146delinsGCTA	ENSP00000299084.4:n.33-149_33-146delinsGCTA
ENST00000561205.1:n.371-149_371-146delinsGCTA
ENST00000561317.1:c.-31-149_-31-146delinsGCTA	ENSP00000453680.1:n.-31-149_-31-146delinsGCTA
NM_152594.2:c.33-149_33-146delinsGCTA	NP_689807.1:n.33-149_33-146delinsGCTA
XM_005254202.2:c.69-149_69-146delinsGCTA	XP_005254259.1:n.69-149_69-146delinsGCTA
XM_005254203.3:c.-15-23017_-15-23014delinsGCTA	XP_005254260.1:n.-15-23017_-15-23014delinsGCTA
XM_011521288.1:c.-31-149_-31-146delinsGCTA	XP_011519590.1:n.-31-149_-31-146delinsGCTA
XM_011521289.1:c.-31-149_-31-146delinsGCTA	XP_011519591.1:n.-31-149_-31-146delinsGCTA
XM_011521290.1:c.-31-149_-31-146delinsGCTA	XP_011519592.1:n.-31-149_-31-146delinsGCTA
XM_005254202.3:c.69-149_69-146delinsGCTA	XP_005254259.1:n.69-149_69-146delinsGCTA
XM_011521289.3:c.-31-149_-31-146delinsGCTA	XP_011519591.1:n.-31-149_-31-146delinsGCTA
NM_152594.3:c.33-149_33-146delinsGCTA MANE Select	NP_689807.1:n.33-149_33-146delinsGCTA