Canonical Allele Identifier: CA391934790

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643825C>A (hg19) ; chr15:g.38351624C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351624C>A , CM000677.2:g.38351624C>A	GRCh38
NC_000015.9:g.38643825C>A , CM000677.1:g.38643825C>A	GRCh37
NC_000015.8:g.36431117C>A	NCBI36
NG_008980.1:g.103774C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.1295C>A MANE Select	ENSP00000299084.4:p.Ala432Glu
ENST00000299084.8:c.1295C>A	ENSP00000299084.4:p.Ala432Glu
NM_152594.2:c.1295C>A	NP_689807.1:p.Ala432Glu
XM_005254202.2:c.1331C>A	XP_005254259.1:p.Ala444Glu
XM_005254203.3:c.1073C>A	XP_005254260.1:p.Ala358Glu
XM_011521288.1:c.1232C>A	XP_011519590.1:p.Ala411Glu
XM_011521289.1:c.1232C>A	XP_011519591.1:p.Ala411Glu
XM_011521290.1:c.1232C>A	XP_011519592.1:p.Ala411Glu
XM_005254202.3:c.1331C>A	XP_005254259.1:p.Ala444Glu
XM_011521289.3:c.1232C>A	XP_011519591.1:p.Ala411Glu
NM_152594.3:c.1295C>A MANE Select	NP_689807.1:p.Ala432Glu