Canonical Allele Identifier: CA391933208

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351102A>G , CM000677.2:g.38351102A>G	GRCh38
NC_000015.9:g.38643303A>G , CM000677.1:g.38643303A>G	GRCh37
NC_000015.8:g.36430595A>G	NCBI36
NG_008980.1:g.103252A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_152594.3:c.773A>G MANE Select	NP_689807.1:p.Tyr258Cys
ENST00000299084.9:c.773A>G MANE Select	ENSP00000299084.4:p.Tyr258Cys
NM_152594.2:c.773A>G	NP_689807.1:p.Tyr258Cys
ENST00000299084.8:c.773A>G	ENSP00000299084.4:p.Tyr258Cys
XM_005254202.2:c.809A>G	XP_005254259.1:p.Tyr270Cys
XM_005254202.3:c.809A>G	XP_005254259.1:p.Tyr270Cys
XM_005254203.3:c.551A>G	XP_005254260.1:p.Tyr184Cys
XM_011521288.1:c.710A>G	XP_011519590.1:p.Tyr237Cys
XM_011521289.1:c.710A>G	XP_011519591.1:p.Tyr237Cys
XM_011521289.3:c.710A>G	XP_011519591.1:p.Tyr237Cys
XM_011521290.1:c.710A>G	XP_011519592.1:p.Tyr237Cys