Canonical Allele Identifier: CA489922784

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591742C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299541C>T , CM000677.2:g.38299541C>T	GRCh38
NC_000015.9:g.38591742C>T , CM000677.1:g.38591742C>T	GRCh37
NC_000015.8:g.36379034C>T	NCBI36
NG_008980.1:g.51691C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.201C>T MANE Select	ENSP00000299084.4:p.Asp67=
ENST00000299084.8:c.201C>T	ENSP00000299084.4:p.Asp67=
ENST00000561205.1:n.539C>T
ENST00000561317.1:c.138C>T	ENSP00000453680.1:p.Asp46=
NM_152594.2:c.201C>T	NP_689807.1:p.Asp67=
XM_005254202.2:c.237C>T	XP_005254259.1:p.Asp79=
XM_005254203.3:c.-15-22700C>T	XP_005254260.1:n.-15-22700C>T
XM_011521288.1:c.138C>T	XP_011519590.1:p.Asp46=
XM_011521289.1:c.138C>T	XP_011519591.1:p.Asp46=
XM_011521290.1:c.138C>T	XP_011519592.1:p.Asp46=
XM_005254202.3:c.237C>T	XP_005254259.1:p.Asp79=
XM_011521289.3:c.138C>T	XP_011519591.1:p.Asp46=
NM_152594.3:c.201C>T MANE Select	NP_689807.1:p.Asp67=