Canonical Allele Identifier: CA2170813113

Gene: SPRED1

Linked Data

• dbSNP Id: rs1888508357

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352324G>A , CM000677.2:g.38352324G>A	GRCh38
NC_000015.9:g.38644525G>A , CM000677.1:g.38644525G>A	GRCh37
NC_000015.8:g.36431817G>A	NCBI36
NG_008980.1:g.104474G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*660G>A MANE Select	ENSP00000299084.4:n.*660G>A
ENST00000299084.8:c.*660G>A	ENSP00000299084.4:n.*660G>A
NM_152594.2:c.*660G>A	NP_689807.1:n.*660G>A
XM_005254202.2:c.*660G>A	XP_005254259.1:n.*660G>A
XM_005254203.3:c.*660G>A	XP_005254260.1:n.*660G>A
XM_011521288.1:c.*660G>A	XP_011519590.1:n.*660G>A
XM_011521289.1:c.*660G>A	XP_011519591.1:n.*660G>A
XM_011521290.1:c.*660G>A	XP_011519592.1:n.*660G>A
XM_005254202.3:c.*660G>A	XP_005254259.1:n.*660G>A
XM_011521289.3:c.*660G>A	XP_011519591.1:n.*660G>A
NM_152594.3:c.*660G>A MANE Select	NP_689807.1:n.*660G>A