Canonical Allele Identifier: CA391934527

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643729T>G (hg19) ; chr15:g.38351528T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351528T>G , CM000677.2:g.38351528T>G	GRCh38
NC_000015.9:g.38643729T>G , CM000677.1:g.38643729T>G	GRCh37
NC_000015.8:g.36431021T>G	NCBI36
NG_008980.1:g.103678T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.1199T>G MANE Select	ENSP00000299084.4:p.Phe400Cys
ENST00000299084.8:c.1199T>G	ENSP00000299084.4:p.Phe400Cys
NM_152594.2:c.1199T>G	NP_689807.1:p.Phe400Cys
XM_005254202.2:c.1235T>G	XP_005254259.1:p.Phe412Cys
XM_005254203.3:c.977T>G	XP_005254260.1:p.Phe326Cys
XM_011521288.1:c.1136T>G	XP_011519590.1:p.Phe379Cys
XM_011521289.1:c.1136T>G	XP_011519591.1:p.Phe379Cys
XM_011521290.1:c.1136T>G	XP_011519592.1:p.Phe379Cys
XM_005254202.3:c.1235T>G	XP_005254259.1:p.Phe412Cys
XM_011521289.3:c.1136T>G	XP_011519591.1:p.Phe379Cys
NM_152594.3:c.1199T>G MANE Select	NP_689807.1:p.Phe400Cys