Canonical Allele Identifier: CA489921686

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38545407T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253206T>C , CM000677.2:g.38253206T>C	GRCh38
NC_000015.9:g.38545407T>C , CM000677.1:g.38545407T>C	GRCh37
NC_000015.8:g.36332699T>C	NCBI36
NG_008980.1:g.5356T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.21T>C MANE Select	ENSP00000299084.4:p.Thr7=
ENST00000299084.8:c.21T>C	ENSP00000299084.4:p.Thr7=
ENST00000561205.1:n.359T>C
ENST00000561317.1:c.-107T>C	ENSP00000453680.1:n.-107T>C
NM_152594.2:c.21T>C	NP_689807.1:p.Thr7=
XM_005254202.2:c.21T>C	XP_005254259.1:p.Thr7=
XM_005254203.3:c.-27T>C	XP_005254260.1:n.-27T>C
XM_005254202.3:c.21T>C	XP_005254259.1:p.Thr7=
XR_001751484.1:n.87+361A>G
NM_152594.3:c.21T>C MANE Select	NP_689807.1:p.Thr7=