Canonical Allele Identifier: CA2067593129

Gene: SPPL3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120798455C= , CM000674.2:g.120798455C=	GRCh38
NC_000012.11:g.121236258C= , CM000674.1:g.121236258C=	GRCh37
NC_000012.10:g.119720641C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353487.7:c.102-6898G= MANE Select	ENSP00000288680.4:n.102-6898G=
ENST00000353487.6:c.102-6898G=	ENSP00000288680.4:n.102-6898G=
ENST00000536996.5:c.-10-6898G=	ENSP00000442484.1:n.-10-6898G=
ENST00000540091.1:c.-10-6898G=	ENSP00000444821.1:n.-10-6898G=
ENST00000543181.5:c.-10-6898G=	ENSP00000446088.1:n.-10-6898G=
ENST00000543608.5:c.-10-6898G=	ENSP00000437603.1:n.-10-6898G=
ENST00000543854.5:c.-69+12354G=	ENSP00000439390.1:n.-69+12354G=
NM_139015.4:c.102-6898G=	NP_620584.2:n.102-6898G=
XM_011537924.1:c.159-6898G=	XP_011536226.1:n.159-6898G=
XM_011537925.1:c.102-6898G=	XP_011536227.1:n.102-6898G=
XM_011537925.2:c.102-6898G=	XP_011536227.1:n.102-6898G=
NM_139015.5:c.102-6898G= MANE Select	NP_620584.2:n.102-6898G=