Canonical Allele Identifier: CA2502798273

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38352185_38352186dup , CM000677.2:g.38352185_38352186dup	GRCh38
NC_000015.9:g.38644386_38644387dup , CM000677.1:g.38644386_38644387dup	GRCh37
NC_000015.8:g.36431678_36431679dup	NCBI36
NG_008980.1:g.104335_104336dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*521_*522dup MANE Select	ENSP00000299084.4:n.*521_*522dup
ENST00000299084.8:c.*521_*522dup	ENSP00000299084.4:n.*521_*522dup
NM_152594.2:c.*521_*522dup	NP_689807.1:n.*521_*522dup
XM_005254202.2:c.*521_*522dup	XP_005254259.1:n.*521_*522dup
XM_005254203.3:c.*521_*522dup	XP_005254260.1:n.*521_*522dup
XM_011521288.1:c.*521_*522dup	XP_011519590.1:n.*521_*522dup
XM_011521289.1:c.*521_*522dup	XP_011519591.1:n.*521_*522dup
XM_011521290.1:c.*521_*522dup	XP_011519592.1:n.*521_*522dup
XM_005254202.3:c.*521_*522dup	XP_005254259.1:n.*521_*522dup
XM_011521289.3:c.*521_*522dup	XP_011519591.1:n.*521_*522dup
NM_152594.3:c.*521_*522dup MANE Select	NP_689807.1:n.*521_*522dup