Canonical Allele Identifier: CA13742087

Gene: SPPL3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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