Canonical Allele Identifier: CA7470186

Gene: SPRED1

Linked Data

• dbSNP Id: rs765684707
• ExAC: 15:38643295 A / G
• gnomAD v2: 15-38643295-A-G
• gnomAD v4: 15-38351094-A-G
• MyVariant Identifiers: chr15:g.38643295A>G (hg19) ; chr15:g.38351094A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351094A>G , CM000677.2:g.38351094A>G	GRCh38
NC_000015.9:g.38643295A>G , CM000677.1:g.38643295A>G	GRCh37
NC_000015.8:g.36430587A>G	NCBI36
NG_008980.1:g.103244A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.765A>G MANE Select	ENSP00000299084.4:p.Ile255Met
ENST00000299084.8:c.765A>G	ENSP00000299084.4:p.Ile255Met
NM_152594.2:c.765A>G	NP_689807.1:p.Ile255Met
XM_005254202.2:c.801A>G	XP_005254259.1:p.Ile267Met
XM_005254203.3:c.543A>G	XP_005254260.1:p.Ile181Met
XM_011521288.1:c.702A>G	XP_011519590.1:p.Ile234Met
XM_011521289.1:c.702A>G	XP_011519591.1:p.Ile234Met
XM_011521290.1:c.702A>G	XP_011519592.1:p.Ile234Met
XM_005254202.3:c.801A>G	XP_005254259.1:p.Ile267Met
XM_011521289.3:c.702A>G	XP_011519591.1:p.Ile234Met
NM_152594.3:c.765A>G MANE Select	NP_689807.1:p.Ile255Met