Canonical Allele Identifier: CA489922641

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591592G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299391G>C , CM000677.2:g.38299391G>C	GRCh38
NC_000015.9:g.38591592G>C , CM000677.1:g.38591592G>C	GRCh37
NC_000015.8:g.36378884G>C	NCBI36
NG_008980.1:g.51541G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.51G>C MANE Select	ENSP00000299084.4:p.Val17=
ENST00000299084.8:c.51G>C	ENSP00000299084.4:p.Val17=
ENST00000561205.1:n.389G>C
ENST00000561317.1:c.-13G>C	ENSP00000453680.1:n.-13G>C
NM_152594.2:c.51G>C	NP_689807.1:p.Val17=
XM_005254202.2:c.87G>C	XP_005254259.1:p.Val29=
XM_005254203.3:c.-15-22850G>C	XP_005254260.1:n.-15-22850G>C
XM_011521288.1:c.-13G>C	XP_011519590.1:n.-13G>C
XM_011521289.1:c.-13G>C	XP_011519591.1:n.-13G>C
XM_011521290.1:c.-13G>C	XP_011519592.1:n.-13G>C
XM_005254202.3:c.87G>C	XP_005254259.1:p.Val29=
XM_011521289.3:c.-13G>C	XP_011519591.1:n.-13G>C
NM_152594.3:c.51G>C MANE Select	NP_689807.1:p.Val17=