Canonical Allele Identifier: CA490011903

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643403C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351202C>T , CM000677.2:g.38351202C>T	GRCh38
NC_000015.9:g.38643403C>T , CM000677.1:g.38643403C>T	GRCh37
NC_000015.8:g.36430695C>T	NCBI36
NG_008980.1:g.103352C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.873C>T MANE Select	ENSP00000299084.4:p.Asp291=
ENST00000299084.8:c.873C>T	ENSP00000299084.4:p.Asp291=
NM_152594.2:c.873C>T	NP_689807.1:p.Asp291=
XM_005254202.2:c.909C>T	XP_005254259.1:p.Asp303=
XM_005254203.3:c.651C>T	XP_005254260.1:p.Asp217=
XM_011521288.1:c.810C>T	XP_011519590.1:p.Asp270=
XM_011521289.1:c.810C>T	XP_011519591.1:p.Asp270=
XM_011521290.1:c.810C>T	XP_011519592.1:p.Asp270=
XM_005254202.3:c.909C>T	XP_005254259.1:p.Asp303=
XM_011521289.3:c.810C>T	XP_011519591.1:p.Asp270=
NM_152594.3:c.873C>T MANE Select	NP_689807.1:p.Asp291=