Canonical Allele Identifier: CA2170789110

Gene: SPRED1

Linked Data

• dbSNP Id: rs1895115471

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299719T>A , CM000677.2:g.38299719T>A	GRCh38
NC_000015.9:g.38591920T>A , CM000677.1:g.38591920T>A	GRCh37
NC_000015.8:g.36379212T>A	NCBI36
NG_008980.1:g.51869T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.207+172T>A MANE Select	ENSP00000299084.4:n.207+172T>A
ENST00000299084.8:c.207+172T>A	ENSP00000299084.4:n.207+172T>A
ENST00000561205.1:n.545+172T>A
ENST00000561317.1:c.144+172T>A	ENSP00000453680.1:n.144+172T>A
NM_152594.2:c.207+172T>A	NP_689807.1:n.207+172T>A
XM_005254202.2:c.243+172T>A	XP_005254259.1:n.243+172T>A
XM_005254203.3:c.-15-22522T>A	XP_005254260.1:n.-15-22522T>A
XM_011521288.1:c.144+172T>A	XP_011519590.1:n.144+172T>A
XM_011521289.1:c.144+172T>A	XP_011519591.1:n.144+172T>A
XM_011521290.1:c.144+172T>A	XP_011519592.1:n.144+172T>A
XM_005254202.3:c.243+172T>A	XP_005254259.1:n.243+172T>A
XM_011521289.3:c.144+172T>A	XP_011519591.1:n.144+172T>A
NM_152594.3:c.207+172T>A MANE Select	NP_689807.1:n.207+172T>A