Canonical Allele Identifier: CA2803804895

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299314_38299316del , CM000677.2:g.38299314_38299316del	GRCh38
NC_000015.9:g.38591515_38591517del , CM000677.1:g.38591515_38591517del	GRCh37
NC_000015.8:g.36378807_36378809del	NCBI36
NG_008980.1:g.51464_51466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-59_33-57del MANE Select	ENSP00000299084.4:n.33-59_33-57del
ENST00000299084.8:c.33-59_33-57del	ENSP00000299084.4:n.33-59_33-57del
ENST00000561205.1:n.371-59_371-57del
ENST00000561317.1:c.-31-59_-31-57del	ENSP00000453680.1:n.-31-59_-31-57del
NM_152594.2:c.33-59_33-57del	NP_689807.1:n.33-59_33-57del
XM_005254202.2:c.69-59_69-57del	XP_005254259.1:n.69-59_69-57del
XM_005254203.3:c.-15-22927_-15-22925del	XP_005254260.1:n.-15-22927_-15-22925del
XM_011521288.1:c.-31-59_-31-57del	XP_011519590.1:n.-31-59_-31-57del
XM_011521289.1:c.-31-59_-31-57del	XP_011519591.1:n.-31-59_-31-57del
XM_011521290.1:c.-31-59_-31-57del	XP_011519592.1:n.-31-59_-31-57del
XM_005254202.3:c.69-59_69-57del	XP_005254259.1:n.69-59_69-57del
XM_011521289.3:c.-31-59_-31-57del	XP_011519591.1:n.-31-59_-31-57del
NM_152594.3:c.33-59_33-57del MANE Select	NP_689807.1:n.33-59_33-57del