Canonical Allele Identifier: CA712588582

Gene: SPRED1

Linked Data

• dbSNP Id: rs1312906999
• gnomAD v3: 15-38253288-T-A
• gnomAD v4: 15-38253288-T-A
• MyVariant Identifiers: chr15:g.38545489T>A (hg19) ; chr15:g.38253288T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253288T>A , CM000677.2:g.38253288T>A	GRCh38
NC_000015.9:g.38545489T>A , CM000677.1:g.38545489T>A	GRCh37
NC_000015.8:g.36332781T>A	NCBI36
NG_008980.1:g.5438T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32+71T>A MANE Select	ENSP00000299084.4:n.32+71T>A
ENST00000299084.8:c.32+71T>A	ENSP00000299084.4:n.32+71T>A
ENST00000561205.1:n.370+71T>A
ENST00000561317.1:c.-96+71T>A	ENSP00000453680.1:n.-96+71T>A
NM_152594.2:c.32+71T>A	NP_689807.1:n.32+71T>A
XM_005254202.2:c.32+71T>A	XP_005254259.1:n.32+71T>A
XM_005254203.3:c.-16+71T>A	XP_005254260.1:n.-16+71T>A
XM_005254202.3:c.32+71T>A	XP_005254259.1:n.32+71T>A
XR_001751484.1:n.87+279A>T
NM_152594.3:c.32+71T>A MANE Select	NP_689807.1:n.32+71T>A