Canonical Allele Identifier: CA968819798

Gene: SPRED1

Linked Data

• dbSNP Id: rs1888625401

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38356524A>C , CM000677.2:g.38356524A>C	GRCh38
NC_000015.9:g.38648725A>C , CM000677.1:g.38648725A>C	GRCh37
NC_000015.8:g.36436017A>C	NCBI36
NG_008980.1:g.108674A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.*4860A>C MANE Select	ENSP00000299084.4:n.*4860A>C
ENST00000299084.8:c.*4860A>C	ENSP00000299084.4:n.*4860A>C
NM_152594.2:c.*4860A>C	NP_689807.1:n.*4860A>C
XM_005254202.3:c.*4860A>C	XP_005254259.1:n.*4860A>C
XM_011521289.3:c.*4860A>C	XP_011519591.1:n.*4860A>C
NM_152594.3:c.*4860A>C MANE Select	NP_689807.1:n.*4860A>C