Canonical Allele Identifier: CA2170788919

Gene: SPRED1

Linked Data

• dbSNP Id: rs1895102529

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299261C>G , CM000677.2:g.38299261C>G	GRCh38
NC_000015.9:g.38591462C>G , CM000677.1:g.38591462C>G	GRCh37
NC_000015.8:g.36378754C>G	NCBI36
NG_008980.1:g.51411C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-112C>G MANE Select	ENSP00000299084.4:n.33-112C>G
ENST00000299084.8:c.33-112C>G	ENSP00000299084.4:n.33-112C>G
ENST00000561205.1:n.371-112C>G
ENST00000561317.1:c.-31-112C>G	ENSP00000453680.1:n.-31-112C>G
NM_152594.2:c.33-112C>G	NP_689807.1:n.33-112C>G
XM_005254202.2:c.69-112C>G	XP_005254259.1:n.69-112C>G
XM_005254203.3:c.-15-22980C>G	XP_005254260.1:n.-15-22980C>G
XM_011521288.1:c.-31-112C>G	XP_011519590.1:n.-31-112C>G
XM_011521289.1:c.-31-112C>G	XP_011519591.1:n.-31-112C>G
XM_011521290.1:c.-31-112C>G	XP_011519592.1:n.-31-112C>G
XM_005254202.3:c.69-112C>G	XP_005254259.1:n.69-112C>G
XM_011521289.3:c.-31-112C>G	XP_011519591.1:n.-31-112C>G
NM_152594.3:c.33-112C>G MANE Select	NP_689807.1:n.33-112C>G