Canonical Allele Identifier: CA2170812728

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351478_38351479delinsAG , CM000677.2:g.38351478_38351479delinsAG	GRCh38
NC_000015.9:g.38643679_38643680delinsAG , CM000677.1:g.38643679_38643680delinsAG	GRCh37
NC_000015.8:g.36430971_36430972delinsAG	NCBI36
NG_008980.1:g.103628_103629delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1149_1150delinsAG MANE Select	ENSP00000299084.4:p.Ser383=
ENST00000299084.8:c.1149_1150delinsAG	ENSP00000299084.4:p.Ser383=
NM_152594.2:c.1149_1150delinsAG	NP_689807.1:p.Ser383=
XM_005254202.2:c.1185_1186delinsAG	XP_005254259.1:p.Ser395=
XM_005254203.3:c.927_928delinsAG	XP_005254260.1:p.Ser309=
XM_011521288.1:c.1086_1087delinsAG	XP_011519590.1:p.Ser362=
XM_011521289.1:c.1086_1087delinsAG	XP_011519591.1:p.Ser362=
XM_011521290.1:c.1086_1087delinsAG	XP_011519592.1:p.Ser362=
XM_005254202.3:c.1185_1186delinsAG	XP_005254259.1:p.Ser395=
XM_011521289.3:c.1086_1087delinsAG	XP_011519591.1:p.Ser362=
NM_152594.3:c.1149_1150delinsAG MANE Select	NP_689807.1:p.Ser383=