Canonical Allele Identifier: CA2170812625

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351228_38351233delinsCTAAGT , CM000677.2:g.38351228_38351233delinsCTAAGT	GRCh38
NC_000015.9:g.38643429_38643434delinsCTAAGT , CM000677.1:g.38643429_38643434delinsCTAAGT	GRCh37
NC_000015.8:g.36430721_36430726delinsCTAAGT	NCBI36
NG_008980.1:g.103378_103383delinsCTAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.899_904delinsCTAAGT MANE Select	ENSP00000299084.4:p.Thr300=
ENST00000299084.8:c.899_904delinsCTAAGT	ENSP00000299084.4:p.Thr300=
NM_152594.2:c.899_904delinsCTAAGT	NP_689807.1:p.Thr300=
XM_005254202.2:c.935_940delinsCTAAGT	XP_005254259.1:p.Thr312=
XM_005254203.3:c.677_682delinsCTAAGT	XP_005254260.1:p.Thr226=
XM_011521288.1:c.836_841delinsCTAAGT	XP_011519590.1:p.Thr279=
XM_011521289.1:c.836_841delinsCTAAGT	XP_011519591.1:p.Thr279=
XM_011521290.1:c.836_841delinsCTAAGT	XP_011519592.1:p.Thr279=
XM_005254202.3:c.935_940delinsCTAAGT	XP_005254259.1:p.Thr312=
XM_011521289.3:c.836_841delinsCTAAGT	XP_011519591.1:p.Thr279=
NM_152594.3:c.899_904delinsCTAAGT MANE Select	NP_689807.1:p.Thr300=