Canonical Allele Identifier: CA7470004

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299521C>T , CM000677.2:g.38299521C>T	GRCh38
NC_000015.9:g.38591722C>T , CM000677.1:g.38591722C>T	GRCh37
NC_000015.8:g.36379014C>T	NCBI36
NG_008980.1:g.51671C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.181C>T MANE Select	ENSP00000299084.4:p.Arg61Cys
ENST00000299084.8:c.181C>T	ENSP00000299084.4:p.Arg61Cys
ENST00000561205.1:n.519C>T
ENST00000561317.1:c.118C>T	ENSP00000453680.1:p.Arg40Cys
NM_152594.2:c.181C>T	NP_689807.1:p.Arg61Cys
XM_005254202.2:c.217C>T	XP_005254259.1:p.Arg73Cys
XM_005254203.3:c.-15-22720C>T	XP_005254260.1:n.-15-22720C>T
XM_011521288.1:c.118C>T	XP_011519590.1:p.Arg40Cys
XM_011521289.1:c.118C>T	XP_011519591.1:p.Arg40Cys
XM_011521290.1:c.118C>T	XP_011519592.1:p.Arg40Cys
XM_005254202.3:c.217C>T	XP_005254259.1:p.Arg73Cys
XM_011521289.3:c.118C>T	XP_011519591.1:p.Arg40Cys
NM_152594.3:c.181C>T MANE Select	NP_689807.1:p.Arg61Cys