Canonical Allele Identifier: CA391934306

Gene: SPRED1

Linked Data

• ClinVar Variation Id: 1992811
• ClinVar RCV Id: RCV002796197
• MyVariant Identifiers: chr15:g.38643672C>G (hg19) ; chr15:g.38351471C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351471C>G , CM000677.2:g.38351471C>G	GRCh38
NC_000015.9:g.38643672C>G , CM000677.1:g.38643672C>G	GRCh37
NC_000015.8:g.36430964C>G	NCBI36
NG_008980.1:g.103621C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1142C>G MANE Select	ENSP00000299084.4:p.Ser381Ter
ENST00000299084.8:c.1142C>G	ENSP00000299084.4:p.Ser381Ter
NM_152594.2:c.1142C>G	NP_689807.1:p.Ser381Ter
XM_005254202.2:c.1178C>G	XP_005254259.1:p.Ser393Ter
XM_005254203.3:c.920C>G	XP_005254260.1:p.Ser307Ter
XM_011521288.1:c.1079C>G	XP_011519590.1:p.Ser360Ter
XM_011521289.1:c.1079C>G	XP_011519591.1:p.Ser360Ter
XM_011521290.1:c.1079C>G	XP_011519592.1:p.Ser360Ter
XM_005254202.3:c.1178C>G	XP_005254259.1:p.Ser393Ter
XM_011521289.3:c.1079C>G	XP_011519591.1:p.Ser360Ter
NM_152594.3:c.1142C>G MANE Select	NP_689807.1:p.Ser381Ter