Canonical Allele Identifier: CA391933398

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643383C>G (hg19) ; chr15:g.38351182C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351182C>G , CM000677.2:g.38351182C>G	GRCh38
NC_000015.9:g.38643383C>G , CM000677.1:g.38643383C>G	GRCh37
NC_000015.8:g.36430675C>G	NCBI36
NG_008980.1:g.103332C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.853C>G MANE Select	ENSP00000299084.4:p.Pro285Ala
ENST00000299084.8:c.853C>G	ENSP00000299084.4:p.Pro285Ala
NM_152594.2:c.853C>G	NP_689807.1:p.Pro285Ala
XM_005254202.2:c.889C>G	XP_005254259.1:p.Pro297Ala
XM_005254203.3:c.631C>G	XP_005254260.1:p.Pro211Ala
XM_011521288.1:c.790C>G	XP_011519590.1:p.Pro264Ala
XM_011521289.1:c.790C>G	XP_011519591.1:p.Pro264Ala
XM_011521290.1:c.790C>G	XP_011519592.1:p.Pro264Ala
XM_005254202.3:c.889C>G	XP_005254259.1:p.Pro297Ala
XM_011521289.3:c.790C>G	XP_011519591.1:p.Pro264Ala
NM_152594.3:c.853C>G MANE Select	NP_689807.1:p.Pro285Ala