Canonical Allele Identifier: CA2170813118

Gene: SPRED1

Linked Data

• dbSNP Id: rs1888508723

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352333_38352337del , CM000677.2:g.38352333_38352337del	GRCh38
NC_000015.9:g.38644534_38644538del , CM000677.1:g.38644534_38644538del	GRCh37
NC_000015.8:g.36431826_36431830del	NCBI36
NG_008980.1:g.104483_104487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*669_*673del MANE Select	ENSP00000299084.4:n.*669_*673del
ENST00000299084.8:c.*669_*673del	ENSP00000299084.4:n.*669_*673del
NM_152594.2:c.*669_*673del	NP_689807.1:n.*669_*673del
XM_005254202.2:c.*669_*673del	XP_005254259.1:n.*669_*673del
XM_005254203.3:c.*669_*673del	XP_005254260.1:n.*669_*673del
XM_011521288.1:c.*669_*673del	XP_011519590.1:n.*669_*673del
XM_011521289.1:c.*669_*673del	XP_011519591.1:n.*669_*673del
XM_011521290.1:c.*669_*673del	XP_011519592.1:n.*669_*673del
XM_005254202.3:c.*669_*673del	XP_005254259.1:n.*669_*673del
XM_011521289.3:c.*669_*673del	XP_011519591.1:n.*669_*673del
NM_152594.3:c.*669_*673del MANE Select	NP_689807.1:n.*669_*673del