Canonical Allele Identifier: CA2170765919

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253258_38253259delinsCT , CM000677.2:g.38253258_38253259delinsCT	GRCh38
NC_000015.9:g.38545459_38545460delinsCT , CM000677.1:g.38545459_38545460delinsCT	GRCh37
NC_000015.8:g.36332751_36332752delinsCT	NCBI36
NG_008980.1:g.5408_5409delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32+41_32+42delinsCT MANE Select	ENSP00000299084.4:n.32+41_32+42delinsCT
ENST00000299084.8:c.32+41_32+42delinsCT	ENSP00000299084.4:n.32+41_32+42delinsCT
ENST00000561205.1:n.370+41_370+42delinsCT
ENST00000561317.1:c.-96+41_-96+42delinsCT	ENSP00000453680.1:n.-96+41_-96+42delinsCT
NM_152594.2:c.32+41_32+42delinsCT	NP_689807.1:n.32+41_32+42delinsCT
XM_005254202.2:c.32+41_32+42delinsCT	XP_005254259.1:n.32+41_32+42delinsCT
XM_005254203.3:c.-16+41_-16+42delinsCT	XP_005254260.1:n.-16+41_-16+42delinsCT
XM_005254202.3:c.32+41_32+42delinsCT	XP_005254259.1:n.32+41_32+42delinsCT
XR_001751484.1:n.87+308_87+309delinsAG
NM_152594.3:c.32+41_32+42delinsCT MANE Select	NP_689807.1:n.32+41_32+42delinsCT