Canonical Allele Identifier: CA712588157

Gene: SPRED1

Linked Data

• dbSNP Id: rs1201516563
• gnomAD v3: 15-38252928-C-T
• gnomAD v4: 15-38252928-C-T
• MyVariant Identifiers: chr15:g.38545129C>T (hg19) ; chr15:g.38252928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252928C>T , CM000677.2:g.38252928C>T	GRCh38
NC_000015.9:g.38545129C>T , CM000677.1:g.38545129C>T	GRCh37
NC_000015.8:g.36332421C>T	NCBI36
NG_008980.1:g.5078C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-258C>T MANE Select	ENSP00000299084.4:n.-258C>T
ENST00000299084.8:c.-258C>T	ENSP00000299084.4:n.-258C>T
ENST00000561205.1:n.81C>T
NM_152594.2:c.-258C>T	NP_689807.1:n.-258C>T
XM_005254202.2:c.-258C>T	XP_005254259.1:n.-258C>T
XM_005254203.3:c.-305C>T	XP_005254260.1:n.-305C>T
XM_005254202.3:c.-258C>T	XP_005254259.1:n.-258C>T
XR_001751484.1:n.87+639G>A
NM_152594.3:c.-258C>T MANE Select	NP_689807.1:n.-258C>T