Canonical Allele Identifier: CA391933013

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643218C>G (hg19) ; chr15:g.38351017C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351017C>G , CM000677.2:g.38351017C>G	GRCh38
NC_000015.9:g.38643218C>G , CM000677.1:g.38643218C>G	GRCh37
NC_000015.8:g.36430510C>G	NCBI36
NG_008980.1:g.103167C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.688C>G MANE Select	ENSP00000299084.4:p.Pro230Ala
ENST00000299084.8:c.688C>G	ENSP00000299084.4:p.Pro230Ala
NM_152594.2:c.688C>G	NP_689807.1:p.Pro230Ala
XM_005254202.2:c.724C>G	XP_005254259.1:p.Pro242Ala
XM_005254203.3:c.466C>G	XP_005254260.1:p.Pro156Ala
XM_011521288.1:c.625C>G	XP_011519590.1:p.Pro209Ala
XM_011521289.1:c.625C>G	XP_011519591.1:p.Pro209Ala
XM_011521290.1:c.625C>G	XP_011519592.1:p.Pro209Ala
XM_005254202.3:c.724C>G	XP_005254259.1:p.Pro242Ala
XM_011521289.3:c.625C>G	XP_011519591.1:p.Pro209Ala
NM_152594.3:c.688C>G MANE Select	NP_689807.1:p.Pro230Ala