Canonical Allele Identifier: CA489921683

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38545404G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253203G>C , CM000677.2:g.38253203G>C	GRCh38
NC_000015.9:g.38545404G>C , CM000677.1:g.38545404G>C	GRCh37
NC_000015.8:g.36332696G>C	NCBI36
NG_008980.1:g.5353G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.18G>C MANE Select	ENSP00000299084.4:p.Ala6=
ENST00000299084.8:c.18G>C	ENSP00000299084.4:p.Ala6=
ENST00000561205.1:n.356G>C
ENST00000561317.1:c.-110G>C	ENSP00000453680.1:n.-110G>C
NM_152594.2:c.18G>C	NP_689807.1:p.Ala6=
XM_005254202.2:c.18G>C	XP_005254259.1:p.Ala6=
XM_005254203.3:c.-30G>C	XP_005254260.1:n.-30G>C
XM_005254202.3:c.18G>C	XP_005254259.1:p.Ala6=
XR_001751484.1:n.87+364C>G
NM_152594.3:c.18G>C MANE Select	NP_689807.1:p.Ala6=