Canonical Allele Identifier: CA2170765451

Gene: SPRED1

Linked Data

• dbSNP Id: rs1894007652
• gnomAD v4: 15-38252865-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252865C>T , CM000677.2:g.38252865C>T	GRCh38
NC_000015.9:g.38545066C>T , CM000677.1:g.38545066C>T	GRCh37
NC_000015.8:g.36332358C>T	NCBI36
NG_008980.1:g.5015C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-321C>T MANE Select	ENSP00000299084.4:n.-321C>T
ENST00000299084.8:c.-321C>T	ENSP00000299084.4:n.-321C>T
ENST00000561205.1:n.18C>T
NM_152594.2:c.-321C>T	NP_689807.1:n.-321C>T
XM_005254202.2:c.-321C>T	XP_005254259.1:n.-321C>T
XM_005254203.3:c.-368C>T	XP_005254260.1:n.-368C>T
XM_005254202.3:c.-321C>T	XP_005254259.1:n.-321C>T
XR_001751484.1:n.87+702G>A
NM_152594.3:c.-321C>T MANE Select	NP_689807.1:n.-321C>T