Canonical Allele Identifier: CA489922881

Gene: SPRED1

Linked Data

• dbSNP Id: rs376226762
• gnomAD v2: 15-38643217-C-G
• gnomAD v3: 15-38351016-C-G
• gnomAD v4: 15-38351016-C-G
• MyVariant Identifiers: chr15:g.38643217C>G (hg19) ; chr15:g.38351016C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351016C>G , CM000677.2:g.38351016C>G	GRCh38
NC_000015.9:g.38643217C>G , CM000677.1:g.38643217C>G	GRCh37
NC_000015.8:g.36430509C>G	NCBI36
NG_008980.1:g.103166C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.687C>G MANE Select	ENSP00000299084.4:p.Val229=
ENST00000299084.8:c.687C>G	ENSP00000299084.4:p.Val229=
NM_152594.2:c.687C>G	NP_689807.1:p.Val229=
XM_005254202.2:c.723C>G	XP_005254259.1:p.Val241=
XM_005254203.3:c.465C>G	XP_005254260.1:p.Val155=
XM_011521288.1:c.624C>G	XP_011519590.1:p.Val208=
XM_011521289.1:c.624C>G	XP_011519591.1:p.Val208=
XM_011521290.1:c.624C>G	XP_011519592.1:p.Val208=
XM_005254202.3:c.723C>G	XP_005254259.1:p.Val241=
XM_011521289.3:c.624C>G	XP_011519591.1:p.Val208=
NM_152594.3:c.687C>G MANE Select	NP_689807.1:p.Val229=