Canonical Allele Identifier: CA490012211

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643649G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351448G>A , CM000677.2:g.38351448G>A	GRCh38
NC_000015.9:g.38643649G>A , CM000677.1:g.38643649G>A	GRCh37
NC_000015.8:g.36430941G>A	NCBI36
NG_008980.1:g.103598G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1119G>A MANE Select	ENSP00000299084.4:p.Glu373=
ENST00000299084.8:c.1119G>A	ENSP00000299084.4:p.Glu373=
NM_152594.2:c.1119G>A	NP_689807.1:p.Glu373=
XM_005254202.2:c.1155G>A	XP_005254259.1:p.Glu385=
XM_005254203.3:c.897G>A	XP_005254260.1:p.Glu299=
XM_011521288.1:c.1056G>A	XP_011519590.1:p.Glu352=
XM_011521289.1:c.1056G>A	XP_011519591.1:p.Glu352=
XM_011521290.1:c.1056G>A	XP_011519592.1:p.Glu352=
XM_005254202.3:c.1155G>A	XP_005254259.1:p.Glu385=
XM_011521289.3:c.1056G>A	XP_011519591.1:p.Glu352=
NM_152594.3:c.1119G>A MANE Select	NP_689807.1:p.Glu373=