Canonical Allele Identifier: CA2061868357

Gene: WSCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108250202_108250229delinsGAGAGAGAGAGAGAGAGACAACAGAGAC , CM000674.2:g.108250202_108250229delinsGAGAGAGAGAGAGAGAGACAACAGAGAC	GRCh38
NC_000012.11:g.108643979_108644006delinsGAGAGAGAGAGAGAGAGACAACAGAGAC , CM000674.1:g.108643979_108644006delinsGAGAGAGAGAGAGAGAGACAACAGAGAC	GRCh37
NC_000012.10:g.107168109_107168136delinsGAGAGAGAGAGAGAGAGACAACAGAGAC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000547525.6:c.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGAC MANE Select	ENSP00000448047.1:n.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAG...
ENST00000332082.8:c.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGAC	ENSP00000331933.4:n.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAG...
NM_001304447.1:c.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGAC	NP_001291376.1:n.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGA...
NM_014653.3:c.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGAC	NP_055468.2:n.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGAC
NM_014653.4:c.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGAC MANE Select	NP_055468.2:n.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGAC
NM_001304447.2:c.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGAC	NP_001291376.1:n.*1859_*1886delinsGAGAGAGAGAGAGAGAGACAACAGAGA...