Canonical Allele Identifier: CA2170812626

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351230_38351234delinsAAGTT , CM000677.2:g.38351230_38351234delinsAAGTT	GRCh38
NC_000015.9:g.38643431_38643435delinsAAGTT , CM000677.1:g.38643431_38643435delinsAAGTT	GRCh37
NC_000015.8:g.36430723_36430727delinsAAGTT	NCBI36
NG_008980.1:g.103380_103384delinsAAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.901_905delinsAAGTT MANE Select	ENSP00000299084.4:p.Lys301=
ENST00000299084.8:c.901_905delinsAAGTT	ENSP00000299084.4:p.Lys301=
NM_152594.2:c.901_905delinsAAGTT	NP_689807.1:p.Lys301=
XM_005254202.2:c.937_941delinsAAGTT	XP_005254259.1:p.Lys313=
XM_005254203.3:c.679_683delinsAAGTT	XP_005254260.1:p.Lys227=
XM_011521288.1:c.838_842delinsAAGTT	XP_011519590.1:p.Lys280=
XM_011521289.1:c.838_842delinsAAGTT	XP_011519591.1:p.Lys280=
XM_011521290.1:c.838_842delinsAAGTT	XP_011519592.1:p.Lys280=
XM_005254202.3:c.937_941delinsAAGTT	XP_005254259.1:p.Lys313=
XM_011521289.3:c.838_842delinsAAGTT	XP_011519591.1:p.Lys280=
NM_152594.3:c.901_905delinsAAGTT MANE Select	NP_689807.1:p.Lys301=