Canonical Allele Identifier: CA2170812729

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351479_38351480delinsGA , CM000677.2:g.38351479_38351480delinsGA	GRCh38
NC_000015.9:g.38643680_38643681delinsGA , CM000677.1:g.38643680_38643681delinsGA	GRCh37
NC_000015.8:g.36430972_36430973delinsGA	NCBI36
NG_008980.1:g.103629_103630delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1150_1151delinsGA MANE Select	ENSP00000299084.4:p.Glu384=
ENST00000299084.8:c.1150_1151delinsGA	ENSP00000299084.4:p.Glu384=
NM_152594.2:c.1150_1151delinsGA	NP_689807.1:p.Glu384=
XM_005254202.2:c.1186_1187delinsGA	XP_005254259.1:p.Glu396=
XM_005254203.3:c.928_929delinsGA	XP_005254260.1:p.Glu310=
XM_011521288.1:c.1087_1088delinsGA	XP_011519590.1:p.Glu363=
XM_011521289.1:c.1087_1088delinsGA	XP_011519591.1:p.Glu363=
XM_011521290.1:c.1087_1088delinsGA	XP_011519592.1:p.Glu363=
XM_005254202.3:c.1186_1187delinsGA	XP_005254259.1:p.Glu396=
XM_011521289.3:c.1087_1088delinsGA	XP_011519591.1:p.Glu363=
NM_152594.3:c.1150_1151delinsGA MANE Select	NP_689807.1:p.Glu384=