Canonical Allele Identifier: CA490012566

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643749C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351548C>T , CM000677.2:g.38351548C>T	GRCh38
NC_000015.9:g.38643749C>T , CM000677.1:g.38643749C>T	GRCh37
NC_000015.8:g.36431041C>T	NCBI36
NG_008980.1:g.103698C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1219C>T MANE Select	ENSP00000299084.4:p.Leu407=
ENST00000299084.8:c.1219C>T	ENSP00000299084.4:p.Leu407=
NM_152594.2:c.1219C>T	NP_689807.1:p.Leu407=
XM_005254202.2:c.1255C>T	XP_005254259.1:p.Leu419=
XM_005254203.3:c.997C>T	XP_005254260.1:p.Leu333=
XM_011521288.1:c.1156C>T	XP_011519590.1:p.Leu386=
XM_011521289.1:c.1156C>T	XP_011519591.1:p.Leu386=
XM_011521290.1:c.1156C>T	XP_011519592.1:p.Leu386=
XM_005254202.3:c.1255C>T	XP_005254259.1:p.Leu419=
XM_011521289.3:c.1156C>T	XP_011519591.1:p.Leu386=
NM_152594.3:c.1219C>T MANE Select	NP_689807.1:p.Leu407=