Canonical Allele Identifier: CA2575673200

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322152_38322157del , CM000677.2:g.38322152_38322157del	GRCh38
NC_000015.9:g.38614353_38614358del , CM000677.1:g.38614353_38614358del	GRCh37
NC_000015.8:g.36401645_36401650del	NCBI36
NG_008980.1:g.74302_74307del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.208-89_208-84del MANE Select	ENSP00000299084.4:n.208-89_208-84del
ENST00000299084.8:c.208-89_208-84del	ENSP00000299084.4:n.208-89_208-84del
ENST00000561205.1:n.546-89_546-84del
ENST00000561317.1:c.145-89_145-84del	ENSP00000453680.1:n.145-89_145-84del
NM_152594.2:c.208-89_208-84del	NP_689807.1:n.208-89_208-84del
XM_005254202.2:c.244-89_244-84del	XP_005254259.1:n.244-89_244-84del
XM_005254203.3:c.-15-89_-15-84del	XP_005254260.1:n.-15-89_-15-84del
XM_011521288.1:c.145-89_145-84del	XP_011519590.1:n.145-89_145-84del
XM_011521289.1:c.145-89_145-84del	XP_011519591.1:n.145-89_145-84del
XM_011521290.1:c.145-89_145-84del	XP_011519592.1:n.145-89_145-84del
XM_005254202.3:c.244-89_244-84del	XP_005254259.1:n.244-89_244-84del
XM_011521289.3:c.145-89_145-84del	XP_011519591.1:n.145-89_145-84del
NM_152594.3:c.208-89_208-84del MANE Select	NP_689807.1:n.208-89_208-84del