Canonical Allele Identifier: CA490011875

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643394A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351193A>G , CM000677.2:g.38351193A>G	GRCh38
NC_000015.9:g.38643394A>G , CM000677.1:g.38643394A>G	GRCh37
NC_000015.8:g.36430686A>G	NCBI36
NG_008980.1:g.103343A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.864A>G MANE Select	ENSP00000299084.4:p.Lys288=
ENST00000299084.8:c.864A>G	ENSP00000299084.4:p.Lys288=
NM_152594.2:c.864A>G	NP_689807.1:p.Lys288=
XM_005254202.2:c.900A>G	XP_005254259.1:p.Lys300=
XM_005254203.3:c.642A>G	XP_005254260.1:p.Lys214=
XM_011521288.1:c.801A>G	XP_011519590.1:p.Lys267=
XM_011521289.1:c.801A>G	XP_011519591.1:p.Lys267=
XM_011521290.1:c.801A>G	XP_011519592.1:p.Lys267=
XM_005254202.3:c.900A>G	XP_005254259.1:p.Lys300=
XM_011521289.3:c.801A>G	XP_011519591.1:p.Lys267=
NM_152594.3:c.864A>G MANE Select	NP_689807.1:p.Lys288=