Canonical Allele Identifier: CA2170765904

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253252_38253253delinsCT , CM000677.2:g.38253252_38253253delinsCT	GRCh38
NC_000015.9:g.38545453_38545454delinsCT , CM000677.1:g.38545453_38545454delinsCT	GRCh37
NC_000015.8:g.36332745_36332746delinsCT	NCBI36
NG_008980.1:g.5402_5403delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32+35_32+36delinsCT MANE Select	ENSP00000299084.4:n.32+35_32+36delinsCT
ENST00000299084.8:c.32+35_32+36delinsCT	ENSP00000299084.4:n.32+35_32+36delinsCT
ENST00000561205.1:n.370+35_370+36delinsCT
ENST00000561317.1:c.-96+35_-96+36delinsCT	ENSP00000453680.1:n.-96+35_-96+36delinsCT
NM_152594.2:c.32+35_32+36delinsCT	NP_689807.1:n.32+35_32+36delinsCT
XM_005254202.2:c.32+35_32+36delinsCT	XP_005254259.1:n.32+35_32+36delinsCT
XM_005254203.3:c.-16+35_-16+36delinsCT	XP_005254260.1:n.-16+35_-16+36delinsCT
XM_005254202.3:c.32+35_32+36delinsCT	XP_005254259.1:n.32+35_32+36delinsCT
XR_001751484.1:n.87+314_87+315delinsAG
NM_152594.3:c.32+35_32+36delinsCT MANE Select	NP_689807.1:n.32+35_32+36delinsCT