Canonical Allele Identifier: CA16606660

Gene: SPRED1

Linked Data

• ClinVar Variation Id: 391600
• ClinVar RCV Id: RCV000436953 ; RCV000690209
• dbSNP Id: rs1057524159
• MyVariant Identifiers: chr15:g.38591615A>G (hg19) ; chr15:g.38299414A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299414A>G , CM000677.2:g.38299414A>G	GRCh38
NC_000015.9:g.38591615A>G , CM000677.1:g.38591615A>G	GRCh37
NC_000015.8:g.36378907A>G	NCBI36
NG_008980.1:g.51564A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.74A>G MANE Select	ENSP00000299084.4:p.Asp25Gly
ENST00000299084.8:c.74A>G	ENSP00000299084.4:p.Asp25Gly
ENST00000561205.1:n.412A>G
ENST00000561317.1:c.11A>G	ENSP00000453680.1:p.Asp4Gly
NM_152594.2:c.74A>G	NP_689807.1:p.Asp25Gly
XM_005254202.2:c.110A>G	XP_005254259.1:p.Asp37Gly
XM_005254203.3:c.-15-22827A>G	XP_005254260.1:n.-15-22827A>G
XM_011521288.1:c.11A>G	XP_011519590.1:p.Asp4Gly
XM_011521289.1:c.11A>G	XP_011519591.1:p.Asp4Gly
XM_011521290.1:c.11A>G	XP_011519592.1:p.Asp4Gly
XM_005254202.3:c.110A>G	XP_005254259.1:p.Asp37Gly
XM_011521289.3:c.11A>G	XP_011519591.1:p.Asp4Gly
NM_152594.3:c.74A>G MANE Select	NP_689807.1:p.Asp25Gly