Canonical Allele Identifier: CA655988883

Gene: SPRED1

Linked Data

• COSMIC: COSN15668044

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351698dup , CM000677.2:g.38351698dup	GRCh38
NC_000015.9:g.38643899dup , CM000677.1:g.38643899dup	GRCh37
NC_000015.8:g.36431191dup	NCBI36
NG_008980.1:g.103848dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*34dup MANE Select	ENSP00000299084.4:n.*34dup
ENST00000299084.8:c.*34dup	ENSP00000299084.4:n.*34dup
NM_152594.2:c.*34dup	NP_689807.1:n.*34dup
XM_005254202.2:c.*34dup	XP_005254259.1:n.*34dup
XM_005254203.3:c.*34dup	XP_005254260.1:n.*34dup
XM_011521288.1:c.*34dup	XP_011519590.1:n.*34dup
XM_011521289.1:c.*34dup	XP_011519591.1:n.*34dup
XM_011521290.1:c.*34dup	XP_011519592.1:n.*34dup
XM_005254202.3:c.*34dup	XP_005254259.1:n.*34dup
XM_011521289.3:c.*34dup	XP_011519591.1:n.*34dup
NM_152594.3:c.*34dup MANE Select	NP_689807.1:n.*34dup