Canonical Allele Identifier: CA2170811798

Gene: SPRED1

Linked Data

• dbSNP Id: rs1896205242

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349399_38349413del , CM000677.2:g.38349399_38349413del	GRCh38
NC_000015.9:g.38641600_38641614del , CM000677.1:g.38641600_38641614del	GRCh37
NC_000015.8:g.36428892_36428906del	NCBI36
NG_008980.1:g.101549_101563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.583-23_583-9del MANE Select	ENSP00000299084.4:n.583-23_583-9del
ENST00000299084.8:c.583-23_583-9del	ENSP00000299084.4:n.583-23_583-9del
NM_152594.2:c.583-23_583-9del	NP_689807.1:n.583-23_583-9del
XM_005254202.2:c.619-23_619-9del	XP_005254259.1:n.619-23_619-9del
XM_005254203.3:c.361-23_361-9del	XP_005254260.1:n.361-23_361-9del
XM_011521288.1:c.520-23_520-9del	XP_011519590.1:n.520-23_520-9del
XM_011521289.1:c.520-23_520-9del	XP_011519591.1:n.520-23_520-9del
XM_011521290.1:c.520-23_520-9del	XP_011519592.1:n.520-23_520-9del
XM_005254202.3:c.619-23_619-9del	XP_005254259.1:n.619-23_619-9del
XM_011521289.3:c.520-23_520-9del	XP_011519591.1:n.520-23_520-9del
NM_152594.3:c.583-23_583-9del MANE Select	NP_689807.1:n.583-23_583-9del