Canonical Allele Identifier: CA489922642

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591595A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299394A>C , CM000677.2:g.38299394A>C	GRCh38
NC_000015.9:g.38591595A>C , CM000677.1:g.38591595A>C	GRCh37
NC_000015.8:g.36378887A>C	NCBI36
NG_008980.1:g.51544A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.54A>C MANE Select	ENSP00000299084.4:p.Arg18=
ENST00000299084.8:c.54A>C	ENSP00000299084.4:p.Arg18=
ENST00000561205.1:n.392A>C
ENST00000561317.1:c.-10A>C	ENSP00000453680.1:n.-10A>C
NM_152594.2:c.54A>C	NP_689807.1:p.Arg18=
XM_005254202.2:c.90A>C	XP_005254259.1:p.Arg30=
XM_005254203.3:c.-15-22847A>C	XP_005254260.1:n.-15-22847A>C
XM_011521288.1:c.-10A>C	XP_011519590.1:n.-10A>C
XM_011521289.1:c.-10A>C	XP_011519591.1:n.-10A>C
XM_011521290.1:c.-10A>C	XP_011519592.1:n.-10A>C
XM_005254202.3:c.90A>C	XP_005254259.1:p.Arg30=
XM_011521289.3:c.-10A>C	XP_011519591.1:n.-10A>C
NM_152594.3:c.54A>C MANE Select	NP_689807.1:p.Arg18=