Canonical Allele Identifier: CA2170814991

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38356559_38356565delinsCTTTAAA , CM000677.2:g.38356559_38356565delinsCTTTAAA	GRCh38
NC_000015.9:g.38648760_38648766delinsCTTTAAA , CM000677.1:g.38648760_38648766delinsCTTTAAA	GRCh37
NC_000015.8:g.36436052_36436058delinsCTTTAAA	NCBI36
NG_008980.1:g.108709_108715delinsCTTTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*4895_*4901delinsCTTTAAA MANE Select	ENSP00000299084.4:n.*4895_*4901delinsCTTTAAA
ENST00000299084.8:c.*4895_*4901delinsCTTTAAA	ENSP00000299084.4:n.*4895_*4901delinsCTTTAAA
NM_152594.2:c.*4895_*4901delinsCTTTAAA	NP_689807.1:n.*4895_*4901delinsCTTTAAA
XM_005254202.3:c.*4895_*4901delinsCTTTAAA	XP_005254259.1:n.*4895_*4901delinsCTTTAAA
XM_011521289.3:c.*4895_*4901delinsCTTTAAA	XP_011519591.1:n.*4895_*4901delinsCTTTAAA
NM_152594.3:c.*4895_*4901delinsCTTTAAA MANE Select	NP_689807.1:n.*4895_*4901delinsCTTTAAA