Canonical Allele Identifier: CA391933604

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643479T>G (hg19) ; chr15:g.38351278T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351278T>G , CM000677.2:g.38351278T>G	GRCh38
NC_000015.9:g.38643479T>G , CM000677.1:g.38643479T>G	GRCh37
NC_000015.8:g.36430771T>G	NCBI36
NG_008980.1:g.103428T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.949T>G MANE Select	ENSP00000299084.4:p.Ser317Ala
ENST00000299084.8:c.949T>G	ENSP00000299084.4:p.Ser317Ala
NM_152594.2:c.949T>G	NP_689807.1:p.Ser317Ala
XM_005254202.2:c.985T>G	XP_005254259.1:p.Ser329Ala
XM_005254203.3:c.727T>G	XP_005254260.1:p.Ser243Ala
XM_011521288.1:c.886T>G	XP_011519590.1:p.Ser296Ala
XM_011521289.1:c.886T>G	XP_011519591.1:p.Ser296Ala
XM_011521290.1:c.886T>G	XP_011519592.1:p.Ser296Ala
XM_005254202.3:c.985T>G	XP_005254259.1:p.Ser329Ala
XM_011521289.3:c.886T>G	XP_011519591.1:p.Ser296Ala
NM_152594.3:c.949T>G MANE Select	NP_689807.1:p.Ser317Ala