Canonical Allele Identifier: CA2170813005

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352104_38352106delinsCAA , CM000677.2:g.38352104_38352106delinsCAA	GRCh38
NC_000015.9:g.38644305_38644307delinsCAA , CM000677.1:g.38644305_38644307delinsCAA	GRCh37
NC_000015.8:g.36431597_36431599delinsCAA	NCBI36
NG_008980.1:g.104254_104256delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*440_*442delinsCAA MANE Select	ENSP00000299084.4:n.*440_*442delinsCAA
ENST00000299084.8:c.*440_*442delinsCAA	ENSP00000299084.4:n.*440_*442delinsCAA
NM_152594.2:c.*440_*442delinsCAA	NP_689807.1:n.*440_*442delinsCAA
XM_005254202.2:c.*440_*442delinsCAA	XP_005254259.1:n.*440_*442delinsCAA
XM_005254203.3:c.*440_*442delinsCAA	XP_005254260.1:n.*440_*442delinsCAA
XM_011521288.1:c.*440_*442delinsCAA	XP_011519590.1:n.*440_*442delinsCAA
XM_011521289.1:c.*440_*442delinsCAA	XP_011519591.1:n.*440_*442delinsCAA
XM_011521290.1:c.*440_*442delinsCAA	XP_011519592.1:n.*440_*442delinsCAA
XM_005254202.3:c.*440_*442delinsCAA	XP_005254259.1:n.*440_*442delinsCAA
XM_011521289.3:c.*440_*442delinsCAA	XP_011519591.1:n.*440_*442delinsCAA
NM_152594.3:c.*440_*442delinsCAA MANE Select	NP_689807.1:n.*440_*442delinsCAA