Canonical Allele Identifier: CA490012562

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643748C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351547C>A , CM000677.2:g.38351547C>A	GRCh38
NC_000015.9:g.38643748C>A , CM000677.1:g.38643748C>A	GRCh37
NC_000015.8:g.36431040C>A	NCBI36
NG_008980.1:g.103697C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1218C>A MANE Select	ENSP00000299084.4:p.Ala406=
ENST00000299084.8:c.1218C>A	ENSP00000299084.4:p.Ala406=
NM_152594.2:c.1218C>A	NP_689807.1:p.Ala406=
XM_005254202.2:c.1254C>A	XP_005254259.1:p.Ala418=
XM_005254203.3:c.996C>A	XP_005254260.1:p.Ala332=
XM_011521288.1:c.1155C>A	XP_011519590.1:p.Ala385=
XM_011521289.1:c.1155C>A	XP_011519591.1:p.Ala385=
XM_011521290.1:c.1155C>A	XP_011519592.1:p.Ala385=
XM_005254202.3:c.1254C>A	XP_005254259.1:p.Ala418=
XM_011521289.3:c.1155C>A	XP_011519591.1:p.Ala385=
NM_152594.3:c.1218C>A MANE Select	NP_689807.1:p.Ala406=