Canonical Allele Identifier: CA391931923

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38614461T>G (hg19) ; chr15:g.38322260T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322260T>G , CM000677.2:g.38322260T>G	GRCh38
NC_000015.9:g.38614461T>G , CM000677.1:g.38614461T>G	GRCh37
NC_000015.8:g.36401753T>G	NCBI36
NG_008980.1:g.74410T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.227T>G MANE Select	ENSP00000299084.4:p.Leu76Arg
ENST00000299084.8:c.227T>G	ENSP00000299084.4:p.Leu76Arg
ENST00000561205.1:n.565T>G
ENST00000561317.1:c.164T>G	ENSP00000453680.1:p.Leu55Arg
NM_152594.2:c.227T>G	NP_689807.1:p.Leu76Arg
XM_005254202.2:c.263T>G	XP_005254259.1:p.Leu88Arg
XM_005254203.3:c.5T>G	XP_005254260.1:p.Leu2Arg
XM_011521288.1:c.164T>G	XP_011519590.1:p.Leu55Arg
XM_011521289.1:c.164T>G	XP_011519591.1:p.Leu55Arg
XM_011521290.1:c.164T>G	XP_011519592.1:p.Leu55Arg
XM_005254202.3:c.263T>G	XP_005254259.1:p.Leu88Arg
XM_011521289.3:c.164T>G	XP_011519591.1:p.Leu55Arg
NM_152594.3:c.227T>G MANE Select	NP_689807.1:p.Leu76Arg