Canonical Allele Identifier: CA2803806069

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351339_38351340insGGGGGGGGGGGG , CM000677.2:g.38351339_38351340insGGGGGGGGGGGG	GRCh38
NC_000015.9:g.38643540_38643541insGGGGGGGGGGGG , CM000677.1:g.38643540_38643541insGGGGGGGGGGGG	GRCh37
NC_000015.8:g.36430832_36430833insGGGGGGGGGGGG	NCBI36
NG_008980.1:g.103489_103490insGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1010_1011insGGGGGGGGGGGG MANE Select	ENSP00000299084.4:p.Tyr337Ter
ENST00000299084.8:c.1010_1011insGGGGGGGGGGGG	ENSP00000299084.4:p.Tyr337Ter
NM_152594.2:c.1010_1011insGGGGGGGGGGGG	NP_689807.1:p.Tyr337Ter
XM_005254202.2:c.1046_1047insGGGGGGGGGGGG	XP_005254259.1:p.Tyr349Ter
XM_005254203.3:c.788_789insGGGGGGGGGGGG	XP_005254260.1:p.Tyr263Ter
XM_011521288.1:c.947_948insGGGGGGGGGGGG	XP_011519590.1:p.Tyr316Ter
XM_011521289.1:c.947_948insGGGGGGGGGGGG	XP_011519591.1:p.Tyr316Ter
XM_011521290.1:c.947_948insGGGGGGGGGGGG	XP_011519592.1:p.Tyr316Ter
XM_005254202.3:c.1046_1047insGGGGGGGGGGGG	XP_005254259.1:p.Tyr349Ter
XM_011521289.3:c.947_948insGGGGGGGGGGGG	XP_011519591.1:p.Tyr316Ter
NM_152594.3:c.1010_1011insGGGGGGGGGGGG MANE Select	NP_689807.1:p.Tyr337Ter