Canonical Allele Identifier: CA2170765807

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253190_38253204delinsGCGAGGAGACGGCGA , CM000677.2:g.38253190_38253204delinsGCGAGGAGACGGCGA	GRCh38
NC_000015.9:g.38545391_38545405delinsGCGAGGAGACGGCGA , CM000677.1:g.38545391_38545405delinsGCGAGGAGACGGCGA	GRCh37
NC_000015.8:g.36332683_36332697delinsGCGAGGAGACGGCGA	NCBI36
NG_008980.1:g.5340_5354delinsGCGAGGAGACGGCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.5_19delinsGCGAGGAGACGGCGA MANE Select	ENSP00000299084.4:p.Ser2=
ENST00000299084.8:c.5_19delinsGCGAGGAGACGGCGA	ENSP00000299084.4:p.Ser2=
ENST00000561205.1:n.343_357delinsGCGAGGAGACGGCGA
ENST00000561317.1:c.-123_-109delinsGCGAGGAGACGGCGA	ENSP00000453680.1:n.-123_-109delinsGCGAGGAGACGGCGA
NM_152594.2:c.5_19delinsGCGAGGAGACGGCGA	NP_689807.1:p.Ser2=
XM_005254202.2:c.5_19delinsGCGAGGAGACGGCGA	XP_005254259.1:p.Ser2=
XM_005254203.3:c.-43_-29delinsGCGAGGAGACGGCGA	XP_005254260.1:n.-43_-29delinsGCGAGGAGACGGCGA
XM_005254202.3:c.5_19delinsGCGAGGAGACGGCGA	XP_005254259.1:p.Ser2=
XR_001751484.1:n.87+363_87+377delinsTCGCCGTCTCCTCGC
NM_152594.3:c.5_19delinsGCGAGGAGACGGCGA MANE Select	NP_689807.1:p.Ser2=