Canonical Allele Identifier: CA2627716241

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38351753-A-ATTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351753_38351754insTTCC , CM000677.2:g.38351753_38351754insTTCC	GRCh38
NC_000015.9:g.38643954_38643955insTTCC , CM000677.1:g.38643954_38643955insTTCC	GRCh37
NC_000015.8:g.36431246_36431247insTTCC	NCBI36
NG_008980.1:g.103903_103904insTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*89_*90insTTCC MANE Select	ENSP00000299084.4:n.*89_*90insTTCC
ENST00000299084.8:c.*89_*90insTTCC	ENSP00000299084.4:n.*89_*90insTTCC
NM_152594.2:c.*89_*90insTTCC	NP_689807.1:n.*89_*90insTTCC
XM_005254202.2:c.*89_*90insTTCC	XP_005254259.1:n.*89_*90insTTCC
XM_005254203.3:c.*89_*90insTTCC	XP_005254260.1:n.*89_*90insTTCC
XM_011521288.1:c.*89_*90insTTCC	XP_011519590.1:n.*89_*90insTTCC
XM_011521289.1:c.*89_*90insTTCC	XP_011519591.1:n.*89_*90insTTCC
XM_011521290.1:c.*89_*90insTTCC	XP_011519592.1:n.*89_*90insTTCC
XM_005254202.3:c.*89_*90insTTCC	XP_005254259.1:n.*89_*90insTTCC
XM_011521289.3:c.*89_*90insTTCC	XP_011519591.1:n.*89_*90insTTCC
NM_152594.3:c.*89_*90insTTCC MANE Select	NP_689807.1:n.*89_*90insTTCC