Canonical Allele Identifier: CA391934045

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591639C>A (hg19) ; chr15:g.38299438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299438C>A , CM000677.2:g.38299438C>A	GRCh38
NC_000015.9:g.38591639C>A , CM000677.1:g.38591639C>A	GRCh37
NC_000015.8:g.36378931C>A	NCBI36
NG_008980.1:g.51588C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.98C>A MANE Select	ENSP00000299084.4:p.Pro33Gln
ENST00000299084.8:c.98C>A	ENSP00000299084.4:p.Pro33Gln
ENST00000561205.1:n.436C>A
ENST00000561317.1:c.35C>A	ENSP00000453680.1:p.Pro12Gln
NM_152594.2:c.98C>A	NP_689807.1:p.Pro33Gln
XM_005254202.2:c.134C>A	XP_005254259.1:p.Pro45Gln
XM_005254203.3:c.-15-22803C>A	XP_005254260.1:n.-15-22803C>A
XM_011521288.1:c.35C>A	XP_011519590.1:p.Pro12Gln
XM_011521289.1:c.35C>A	XP_011519591.1:p.Pro12Gln
XM_011521290.1:c.35C>A	XP_011519592.1:p.Pro12Gln
XM_005254202.3:c.134C>A	XP_005254259.1:p.Pro45Gln
XM_011521289.3:c.35C>A	XP_011519591.1:p.Pro12Gln
NM_152594.3:c.98C>A MANE Select	NP_689807.1:p.Pro33Gln