Canonical Allele Identifier: CA7470036

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322339G>A , CM000677.2:g.38322339G>A	GRCh38
NC_000015.9:g.38614540G>A , CM000677.1:g.38614540G>A	GRCh37
NC_000015.8:g.36401832G>A	NCBI36
NG_008980.1:g.74489G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_152594.3:c.306G>A MANE Select	NP_689807.1:p.Thr102=
ENST00000299084.9:c.306G>A MANE Select	ENSP00000299084.4:p.Thr102=
NM_152594.2:c.306G>A	NP_689807.1:p.Thr102=
ENST00000299084.8:c.306G>A	ENSP00000299084.4:p.Thr102=
ENST00000561205.1:n.644G>A
ENST00000561317.1:c.243G>A	ENSP00000453680.1:p.Thr81=
XM_005254202.2:c.342G>A	XP_005254259.1:p.Thr114=
XM_005254202.3:c.342G>A	XP_005254259.1:p.Thr114=
XM_005254203.3:c.84G>A	XP_005254260.1:p.Thr28=
XM_011521288.1:c.243G>A	XP_011519590.1:p.Thr81=
XM_011521289.1:c.243G>A	XP_011519591.1:p.Thr81=
XM_011521289.3:c.243G>A	XP_011519591.1:p.Thr81=
XM_011521290.1:c.243G>A	XP_011519592.1:p.Thr81=