Canonical Allele Identifier: CA391934282

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591684C>A (hg19) ; chr15:g.38299483C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299483C>A , CM000677.2:g.38299483C>A	GRCh38
NC_000015.9:g.38591684C>A , CM000677.1:g.38591684C>A	GRCh37
NC_000015.8:g.36378976C>A	NCBI36
NG_008980.1:g.51633C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.143C>A MANE Select	ENSP00000299084.4:p.Pro48His
ENST00000299084.8:c.143C>A	ENSP00000299084.4:p.Pro48His
ENST00000561205.1:n.481C>A
ENST00000561317.1:c.80C>A	ENSP00000453680.1:p.Pro27His
NM_152594.2:c.143C>A	NP_689807.1:p.Pro48His
XM_005254202.2:c.179C>A	XP_005254259.1:p.Pro60His
XM_005254203.3:c.-15-22758C>A	XP_005254260.1:n.-15-22758C>A
XM_011521288.1:c.80C>A	XP_011519590.1:p.Pro27His
XM_011521289.1:c.80C>A	XP_011519591.1:p.Pro27His
XM_011521290.1:c.80C>A	XP_011519592.1:p.Pro27His
XM_005254202.3:c.179C>A	XP_005254259.1:p.Pro60His
XM_011521289.3:c.80C>A	XP_011519591.1:p.Pro27His
NM_152594.3:c.143C>A MANE Select	NP_689807.1:p.Pro48His