Canonical Allele Identifier: CA2564237004

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351665_38351666insTC , CM000677.2:g.38351665_38351666insTC	GRCh38
NC_000015.9:g.38643866_38643867insTC , CM000677.1:g.38643866_38643867insTC	GRCh37
NC_000015.8:g.36431158_36431159insTC	NCBI36
NG_008980.1:g.103815_103816insTC

Transcript Alleles

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