Canonical Allele Identifier: CA391933794

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299386C>G , CM000677.2:g.38299386C>G	GRCh38
NC_000015.9:g.38591587C>G , CM000677.1:g.38591587C>G	GRCh37
NC_000015.8:g.36378879C>G	NCBI36
NG_008980.1:g.51536C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_152594.3:c.46C>G MANE Select	NP_689807.1:p.Arg16Gly
ENST00000299084.9:c.46C>G MANE Select	ENSP00000299084.4:p.Arg16Gly
NM_152594.2:c.46C>G	NP_689807.1:p.Arg16Gly
ENST00000299084.8:c.46C>G	ENSP00000299084.4:p.Arg16Gly
ENST00000561205.1:n.384C>G
ENST00000561317.1:c.-18C>G	ENSP00000453680.1:n.-18C>G
XM_005254202.2:c.82C>G	XP_005254259.1:p.Arg28Gly
XM_005254202.3:c.82C>G	XP_005254259.1:p.Arg28Gly
XM_005254203.3:c.-15-22855C>G	XP_005254260.1:n.-15-22855C>G
XM_011521288.1:c.-18C>G	XP_011519590.1:n.-18C>G
XM_011521289.1:c.-18C>G	XP_011519591.1:n.-18C>G
XM_011521289.3:c.-18C>G	XP_011519591.1:n.-18C>G
XM_011521290.1:c.-18C>G	XP_011519592.1:n.-18C>G