Canonical Allele Identifier: CA269287892

Gene: SPRED1

Linked Data

• dbSNP Id: rs144515463
• gnomAD v2: 15-38591524-T-TG
• MyVariant Identifiers: chr15:g.38591524_38591525insG (hg19) ; chr15:g.38299323_38299324insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299324dup , CM000677.2:g.38299324dup	GRCh38
NC_000015.9:g.38591525dup , CM000677.1:g.38591525dup	GRCh37
NC_000015.8:g.36378817dup	NCBI36
NG_008980.1:g.51474dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-49dup MANE Select	ENSP00000299084.4:n.33-49dup
ENST00000299084.8:c.33-49dup	ENSP00000299084.4:n.33-49dup
ENST00000561205.1:n.371-49dup
ENST00000561317.1:c.-31-49dup	ENSP00000453680.1:n.-31-49dup
NM_152594.2:c.33-49dup	NP_689807.1:n.33-49dup
XM_005254202.2:c.69-49dup	XP_005254259.1:n.69-49dup
XM_005254203.3:c.-15-22917dup	XP_005254260.1:n.-15-22917dup
XM_011521288.1:c.-31-49dup	XP_011519590.1:n.-31-49dup
XM_011521289.1:c.-31-49dup	XP_011519591.1:n.-31-49dup
XM_011521290.1:c.-31-49dup	XP_011519592.1:n.-31-49dup
XM_005254202.3:c.69-49dup	XP_005254259.1:n.69-49dup
XM_011521289.3:c.-31-49dup	XP_011519591.1:n.-31-49dup
NM_152594.3:c.33-49dup MANE Select	NP_689807.1:n.33-49dup