Canonical Allele Identifier: CA490011810

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643358T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351157T>G , CM000677.2:g.38351157T>G	GRCh38
NC_000015.9:g.38643358T>G , CM000677.1:g.38643358T>G	GRCh37
NC_000015.8:g.36430650T>G	NCBI36
NG_008980.1:g.103307T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.828T>G MANE Select	ENSP00000299084.4:p.Ala276=
ENST00000299084.8:c.828T>G	ENSP00000299084.4:p.Ala276=
NM_152594.2:c.828T>G	NP_689807.1:p.Ala276=
XM_005254202.2:c.864T>G	XP_005254259.1:p.Ala288=
XM_005254203.3:c.606T>G	XP_005254260.1:p.Ala202=
XM_011521288.1:c.765T>G	XP_011519590.1:p.Ala255=
XM_011521289.1:c.765T>G	XP_011519591.1:p.Ala255=
XM_011521290.1:c.765T>G	XP_011519592.1:p.Ala255=
XM_005254202.3:c.864T>G	XP_005254259.1:p.Ala288=
XM_011521289.3:c.765T>G	XP_011519591.1:p.Ala255=
NM_152594.3:c.828T>G MANE Select	NP_689807.1:p.Ala276=