Canonical Allele Identifier: CA490012415

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643538A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351337A>T , CM000677.2:g.38351337A>T	GRCh38
NC_000015.9:g.38643538A>T , CM000677.1:g.38643538A>T	GRCh37
NC_000015.8:g.36430830A>T	NCBI36
NG_008980.1:g.103487A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1008A>T MANE Select	ENSP00000299084.4:p.Val336=
ENST00000299084.8:c.1008A>T	ENSP00000299084.4:p.Val336=
NM_152594.2:c.1008A>T	NP_689807.1:p.Val336=
XM_005254202.2:c.1044A>T	XP_005254259.1:p.Val348=
XM_005254203.3:c.786A>T	XP_005254260.1:p.Val262=
XM_011521288.1:c.945A>T	XP_011519590.1:p.Val315=
XM_011521289.1:c.945A>T	XP_011519591.1:p.Val315=
XM_011521290.1:c.945A>T	XP_011519592.1:p.Val315=
XM_005254202.3:c.1044A>T	XP_005254259.1:p.Val348=
XM_011521289.3:c.945A>T	XP_011519591.1:p.Val315=
NM_152594.3:c.1008A>T MANE Select	NP_689807.1:p.Val336=