Canonical Allele Identifier: CA490012443

Gene: SPRED1

Linked Data

• dbSNP Id: rs1405547941
• MyVariant Identifiers: chr15:g.38643553G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351352G>A , CM000677.2:g.38351352G>A	GRCh38
NC_000015.9:g.38643553G>A , CM000677.1:g.38643553G>A	GRCh37
NC_000015.8:g.36430845G>A	NCBI36
NG_008980.1:g.103502G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1023G>A MANE Select	ENSP00000299084.4:p.Arg341=
ENST00000299084.8:c.1023G>A	ENSP00000299084.4:p.Arg341=
NM_152594.2:c.1023G>A	NP_689807.1:p.Arg341=
XM_005254202.2:c.1059G>A	XP_005254259.1:p.Arg353=
XM_005254203.3:c.801G>A	XP_005254260.1:p.Arg267=
XM_011521288.1:c.960G>A	XP_011519590.1:p.Arg320=
XM_011521289.1:c.960G>A	XP_011519591.1:p.Arg320=
XM_011521290.1:c.960G>A	XP_011519592.1:p.Arg320=
XM_005254202.3:c.1059G>A	XP_005254259.1:p.Arg353=
XM_011521289.3:c.960G>A	XP_011519591.1:p.Arg320=
NM_152594.3:c.1023G>A MANE Select	NP_689807.1:p.Arg341=