Canonical Allele Identifier: CA919534453

Gene: SPRED1

Linked Data

• dbSNP Id: rs1595746677

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322173_38322176del , CM000677.2:g.38322173_38322176del	GRCh38
NC_000015.9:g.38614374_38614377del , CM000677.1:g.38614374_38614377del	GRCh37
NC_000015.8:g.36401666_36401669del	NCBI36
NG_008980.1:g.74323_74326del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.208-68_208-65del MANE Select	ENSP00000299084.4:n.208-68_208-65del
ENST00000299084.8:c.208-68_208-65del	ENSP00000299084.4:n.208-68_208-65del
ENST00000561205.1:n.546-68_546-65del
ENST00000561317.1:c.145-68_145-65del	ENSP00000453680.1:n.145-68_145-65del
NM_152594.2:c.208-68_208-65del	NP_689807.1:n.208-68_208-65del
XM_005254202.2:c.244-68_244-65del	XP_005254259.1:n.244-68_244-65del
XM_005254203.3:c.-15-68_-15-65del	XP_005254260.1:n.-15-68_-15-65del
XM_011521288.1:c.145-68_145-65del	XP_011519590.1:n.145-68_145-65del
XM_011521289.1:c.145-68_145-65del	XP_011519591.1:n.145-68_145-65del
XM_011521290.1:c.145-68_145-65del	XP_011519592.1:n.145-68_145-65del
XM_005254202.3:c.244-68_244-65del	XP_005254259.1:n.244-68_244-65del
XM_011521289.3:c.145-68_145-65del	XP_011519591.1:n.145-68_145-65del
NM_152594.3:c.208-68_208-65del MANE Select	NP_689807.1:n.208-68_208-65del