Canonical Allele Identifier: CA2627715275

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38322154-CGTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322157_38322159del , CM000677.2:g.38322157_38322159del	GRCh38
NC_000015.9:g.38614358_38614360del , CM000677.1:g.38614358_38614360del	GRCh37
NC_000015.8:g.36401650_36401652del	NCBI36
NG_008980.1:g.74307_74309del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.208-84_208-82del MANE Select	ENSP00000299084.4:n.208-84_208-82del
ENST00000299084.8:c.208-84_208-82del	ENSP00000299084.4:n.208-84_208-82del
ENST00000561205.1:n.546-84_546-82del
ENST00000561317.1:c.145-84_145-82del	ENSP00000453680.1:n.145-84_145-82del
NM_152594.2:c.208-84_208-82del	NP_689807.1:n.208-84_208-82del
XM_005254202.2:c.244-84_244-82del	XP_005254259.1:n.244-84_244-82del
XM_005254203.3:c.-15-84_-15-82del	XP_005254260.1:n.-15-84_-15-82del
XM_011521288.1:c.145-84_145-82del	XP_011519590.1:n.145-84_145-82del
XM_011521289.1:c.145-84_145-82del	XP_011519591.1:n.145-84_145-82del
XM_011521290.1:c.145-84_145-82del	XP_011519592.1:n.145-84_145-82del
XM_005254202.3:c.244-84_244-82del	XP_005254259.1:n.244-84_244-82del
XM_011521289.3:c.145-84_145-82del	XP_011519591.1:n.145-84_145-82del
NM_152594.3:c.208-84_208-82del MANE Select	NP_689807.1:n.208-84_208-82del