Canonical Allele Identifier: CA13271487

Gene: WAPL

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86456645G>A , CM000672.2:g.86456645G>A	GRCh38
NC_000010.10:g.88216402G>A , CM000672.1:g.88216402G>A	GRCh37
NC_000010.9:g.88206382G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298767.10:c.2657+2344C>T MANE Select	ENSP00000298767.4:n.2657+2344C>T
ENST00000372075.2:c.515+2344C>T	ENSP00000361145.2:n.515+2344C>T
ENST00000263070.11:c.458+2344C>T	ENSP00000263070.7:n.458+2344C>T
ENST00000298767.9:c.2657+2344C>T	ENSP00000298767.4:n.2657+2344C>T
ENST00000372075.1:c.458+2344C>T	ENSP00000361145.1:n.458+2344C>T
ENST00000618527.4:c.2657+2344C>T	ENSP00000481451.1:n.2657+2344C>T
NM_015045.2:c.2657+2344C>T	NP_055860.1:n.2657+2344C>T
XM_006717729.2:c.2639+2344C>T	XP_006717792.1:n.2639+2344C>T
XM_011539547.1:c.2522+2344C>T	XP_011537849.1:n.2522+2344C>T
XM_011539548.1:c.2675+2344C>T	XP_011537850.1:n.2675+2344C>T
NM_001318328.1:c.2639+2344C>T	NP_001305257.1:n.2639+2344C>T
NM_015045.3:c.2657+2344C>T	NP_055860.1:n.2657+2344C>T
XM_017015979.1:c.2522+2344C>T	XP_016871468.1:n.2522+2344C>T
XM_017015980.1:c.2504+2344C>T	XP_016871469.1:n.2504+2344C>T
XM_017015981.1:c.1016+2344C>T	XP_016871470.1:n.1016+2344C>T
NM_015045.4:c.2657+2344C>T	NP_055860.1:n.2657+2344C>T
NM_015045.5:c.2657+2344C>T MANE Select	NP_055860.1:n.2657+2344C>T
NM_001318328.2:c.2639+2344C>T	NP_001305257.1:n.2639+2344C>T