Canonical Allele Identifier: CA2170811771

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349366_38349370delinsGTTTC , CM000677.2:g.38349366_38349370delinsGTTTC	GRCh38
NC_000015.9:g.38641567_38641571delinsGTTTC , CM000677.1:g.38641567_38641571delinsGTTTC	GRCh37
NC_000015.8:g.36428859_36428863delinsGTTTC	NCBI36
NG_008980.1:g.101516_101520delinsGTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.583-56_583-52delinsGTTTC MANE Select	ENSP00000299084.4:n.583-56_583-52delinsGTTTC
ENST00000299084.8:c.583-56_583-52delinsGTTTC	ENSP00000299084.4:n.583-56_583-52delinsGTTTC
NM_152594.2:c.583-56_583-52delinsGTTTC	NP_689807.1:n.583-56_583-52delinsGTTTC
XM_005254202.2:c.619-56_619-52delinsGTTTC	XP_005254259.1:n.619-56_619-52delinsGTTTC
XM_005254203.3:c.361-56_361-52delinsGTTTC	XP_005254260.1:n.361-56_361-52delinsGTTTC
XM_011521288.1:c.520-56_520-52delinsGTTTC	XP_011519590.1:n.520-56_520-52delinsGTTTC
XM_011521289.1:c.520-56_520-52delinsGTTTC	XP_011519591.1:n.520-56_520-52delinsGTTTC
XM_011521290.1:c.520-56_520-52delinsGTTTC	XP_011519592.1:n.520-56_520-52delinsGTTTC
XM_005254202.3:c.619-56_619-52delinsGTTTC	XP_005254259.1:n.619-56_619-52delinsGTTTC
XM_011521289.3:c.520-56_520-52delinsGTTTC	XP_011519591.1:n.520-56_520-52delinsGTTTC
NM_152594.3:c.583-56_583-52delinsGTTTC MANE Select	NP_689807.1:n.583-56_583-52delinsGTTTC