Canonical Allele Identifier: CA712588142

Gene: SPRED1

Linked Data

• dbSNP Id: rs1200356160
• gnomAD v3: 15-38252912-C-T
• gnomAD v4: 15-38252912-C-T
• MyVariant Identifiers: chr15:g.38545113C>T (hg19) ; chr15:g.38252912C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252912C>T , CM000677.2:g.38252912C>T	GRCh38
NC_000015.9:g.38545113C>T , CM000677.1:g.38545113C>T	GRCh37
NC_000015.8:g.36332405C>T	NCBI36
NG_008980.1:g.5062C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-274C>T MANE Select	ENSP00000299084.4:n.-274C>T
ENST00000299084.8:c.-274C>T	ENSP00000299084.4:n.-274C>T
ENST00000561205.1:n.65C>T
NM_152594.2:c.-274C>T	NP_689807.1:n.-274C>T
XM_005254202.2:c.-274C>T	XP_005254259.1:n.-274C>T
XM_005254203.3:c.-321C>T	XP_005254260.1:n.-321C>T
XM_005254202.3:c.-274C>T	XP_005254259.1:n.-274C>T
XR_001751484.1:n.87+655G>A
NM_152594.3:c.-274C>T MANE Select	NP_689807.1:n.-274C>T