Canonical Allele Identifier: CA489922934

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643292A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351091A>G , CM000677.2:g.38351091A>G	GRCh38
NC_000015.9:g.38643292A>G , CM000677.1:g.38643292A>G	GRCh37
NC_000015.8:g.36430584A>G	NCBI36
NG_008980.1:g.103241A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.762A>G MANE Select	ENSP00000299084.4:p.Leu254=
ENST00000299084.8:c.762A>G	ENSP00000299084.4:p.Leu254=
NM_152594.2:c.762A>G	NP_689807.1:p.Leu254=
XM_005254202.2:c.798A>G	XP_005254259.1:p.Leu266=
XM_005254203.3:c.540A>G	XP_005254260.1:p.Leu180=
XM_011521288.1:c.699A>G	XP_011519590.1:p.Leu233=
XM_011521289.1:c.699A>G	XP_011519591.1:p.Leu233=
XM_011521290.1:c.699A>G	XP_011519592.1:p.Leu233=
XM_005254202.3:c.798A>G	XP_005254259.1:p.Leu266=
XM_011521289.3:c.699A>G	XP_011519591.1:p.Leu233=
NM_152594.3:c.762A>G MANE Select	NP_689807.1:p.Leu254=