Canonical Allele Identifier: CA391933400

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643384C>A (hg19) ; chr15:g.38351183C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351183C>A , CM000677.2:g.38351183C>A	GRCh38
NC_000015.9:g.38643384C>A , CM000677.1:g.38643384C>A	GRCh37
NC_000015.8:g.36430676C>A	NCBI36
NG_008980.1:g.103333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.854C>A MANE Select	ENSP00000299084.4:p.Pro285Gln
ENST00000299084.8:c.854C>A	ENSP00000299084.4:p.Pro285Gln
NM_152594.2:c.854C>A	NP_689807.1:p.Pro285Gln
XM_005254202.2:c.890C>A	XP_005254259.1:p.Pro297Gln
XM_005254203.3:c.632C>A	XP_005254260.1:p.Pro211Gln
XM_011521288.1:c.791C>A	XP_011519590.1:p.Pro264Gln
XM_011521289.1:c.791C>A	XP_011519591.1:p.Pro264Gln
XM_011521290.1:c.791C>A	XP_011519592.1:p.Pro264Gln
XM_005254202.3:c.890C>A	XP_005254259.1:p.Pro297Gln
XM_011521289.3:c.791C>A	XP_011519591.1:p.Pro264Gln
NM_152594.3:c.854C>A MANE Select	NP_689807.1:p.Pro285Gln