Canonical Allele Identifier: CA391931858

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38253217-A-G
• MyVariant Identifiers: chr15:g.38545418A>G (hg19) ; chr15:g.38253217A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253217A>G , CM000677.2:g.38253217A>G	GRCh38
NC_000015.9:g.38545418A>G , CM000677.1:g.38545418A>G	GRCh37
NC_000015.8:g.36332710A>G	NCBI36
NG_008980.1:g.5367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32A>G MANE Select	ENSP00000299084.4:p.Asp11Gly
ENST00000299084.8:c.32A>G	ENSP00000299084.4:p.Asp11Gly
ENST00000561205.1:n.370A>G
ENST00000561317.1:c.-96A>G	ENSP00000453680.1:n.-96A>G
NM_152594.2:c.32A>G	NP_689807.1:p.Asp11Gly
XM_005254202.2:c.32A>G	XP_005254259.1:p.Glu11Gly
XM_005254203.3:c.-16A>G	XP_005254260.1:n.-16A>G
XM_005254202.3:c.32A>G	XP_005254259.1:p.Glu11Gly
XR_001751484.1:n.87+350T>C
NM_152594.3:c.32A>G MANE Select	NP_689807.1:p.Asp11Gly