Canonical Allele Identifier: CA490012660

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643820T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351619T>C , CM000677.2:g.38351619T>C	GRCh38
NC_000015.9:g.38643820T>C , CM000677.1:g.38643820T>C	GRCh37
NC_000015.8:g.36431112T>C	NCBI36
NG_008980.1:g.103769T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1290T>C MANE Select	ENSP00000299084.4:p.Gly430=
ENST00000299084.8:c.1290T>C	ENSP00000299084.4:p.Gly430=
NM_152594.2:c.1290T>C	NP_689807.1:p.Gly430=
XM_005254202.2:c.1326T>C	XP_005254259.1:p.Gly442=
XM_005254203.3:c.1068T>C	XP_005254260.1:p.Gly356=
XM_011521288.1:c.1227T>C	XP_011519590.1:p.Gly409=
XM_011521289.1:c.1227T>C	XP_011519591.1:p.Gly409=
XM_011521290.1:c.1227T>C	XP_011519592.1:p.Gly409=
XM_005254202.3:c.1326T>C	XP_005254259.1:p.Gly442=
XM_011521289.3:c.1227T>C	XP_011519591.1:p.Gly409=
NM_152594.3:c.1290T>C MANE Select	NP_689807.1:p.Gly430=