Canonical Allele Identifier: CA2061868588

Gene: WSCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108250444C= , CM000674.2:g.108250444C=	GRCh38
NC_000012.11:g.108644221C= , CM000674.1:g.108644221C=	GRCh37
NC_000012.10:g.107168351C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547525.6:c.*2101C= MANE Select	ENSP00000448047.1:n.*2101C=
ENST00000332082.8:c.*2101C=	ENSP00000331933.4:n.*2101C=
NM_001304447.1:c.*2101C=	NP_001291376.1:n.*2101C=
NM_014653.3:c.*2101C=	NP_055468.2:n.*2101C=
NM_014653.4:c.*2101C= MANE Select	NP_055468.2:n.*2101C=
NM_001304447.2:c.*2101C=	NP_001291376.1:n.*2101C=