Canonical Allele Identifier: CA2803804896

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299317_38299318insATA , CM000677.2:g.38299317_38299318insATA	GRCh38
NC_000015.9:g.38591518_38591519insATA , CM000677.1:g.38591518_38591519insATA	GRCh37
NC_000015.8:g.36378810_36378811insATA	NCBI36
NG_008980.1:g.51467_51468insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-56_33-55insATA MANE Select	ENSP00000299084.4:n.33-56_33-55insATA
ENST00000299084.8:c.33-56_33-55insATA	ENSP00000299084.4:n.33-56_33-55insATA
ENST00000561205.1:n.371-56_371-55insATA
ENST00000561317.1:c.-31-56_-31-55insATA	ENSP00000453680.1:n.-31-56_-31-55insATA
NM_152594.2:c.33-56_33-55insATA	NP_689807.1:n.33-56_33-55insATA
XM_005254202.2:c.69-56_69-55insATA	XP_005254259.1:n.69-56_69-55insATA
XM_005254203.3:c.-15-22924_-15-22923insATA	XP_005254260.1:n.-15-22924_-15-22923insATA
XM_011521288.1:c.-31-56_-31-55insATA	XP_011519590.1:n.-31-56_-31-55insATA
XM_011521289.1:c.-31-56_-31-55insATA	XP_011519591.1:n.-31-56_-31-55insATA
XM_011521290.1:c.-31-56_-31-55insATA	XP_011519592.1:n.-31-56_-31-55insATA
XM_005254202.3:c.69-56_69-55insATA	XP_005254259.1:n.69-56_69-55insATA
XM_011521289.3:c.-31-56_-31-55insATA	XP_011519591.1:n.-31-56_-31-55insATA
NM_152594.3:c.33-56_33-55insATA MANE Select	NP_689807.1:n.33-56_33-55insATA