Canonical Allele Identifier: CA2627715135

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38299272-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299273_38299274del , CM000677.2:g.38299273_38299274del	GRCh38
NC_000015.9:g.38591474_38591475del , CM000677.1:g.38591474_38591475del	GRCh37
NC_000015.8:g.36378766_36378767del	NCBI36
NG_008980.1:g.51423_51424del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.33-100_33-99del MANE Select	ENSP00000299084.4:n.33-100_33-99del
ENST00000299084.8:c.33-100_33-99del	ENSP00000299084.4:n.33-100_33-99del
ENST00000561205.1:n.371-100_371-99del
ENST00000561317.1:c.-31-100_-31-99del	ENSP00000453680.1:n.-31-100_-31-99del
NM_152594.2:c.33-100_33-99del	NP_689807.1:n.33-100_33-99del
XM_005254202.2:c.69-100_69-99del	XP_005254259.1:n.69-100_69-99del
XM_005254203.3:c.-15-22968_-15-22967del	XP_005254260.1:n.-15-22968_-15-22967del
XM_011521288.1:c.-31-100_-31-99del	XP_011519590.1:n.-31-100_-31-99del
XM_011521289.1:c.-31-100_-31-99del	XP_011519591.1:n.-31-100_-31-99del
XM_011521290.1:c.-31-100_-31-99del	XP_011519592.1:n.-31-100_-31-99del
XM_005254202.3:c.69-100_69-99del	XP_005254259.1:n.69-100_69-99del
XM_011521289.3:c.-31-100_-31-99del	XP_011519591.1:n.-31-100_-31-99del
NM_152594.3:c.33-100_33-99del MANE Select	NP_689807.1:n.33-100_33-99del