Canonical Allele Identifier: CA691993948

Gene: NAP1L1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.76083176A>T , CM000674.2:g.76083176A>T	GRCh38
NC_000012.11:g.76476956A>T , CM000674.1:g.76476956A>T	GRCh37
NC_000012.10:g.74763223A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000618691.5:c.-21+1391T>A MANE Select	ENSP00000477538.1:n.-21+1391T>A
ENST00000261182.12:c.-21+1391T>A	ENSP00000261182.8:n.-21+1391T>A
ENST00000393263.7:c.-21+1391T>A	ENSP00000376947.3:n.-21+1391T>A
ENST00000431879.7:c.-107+1391T>A	ENSP00000409795.3:n.-107+1391T>A
ENST00000535020.6:c.-21+1391T>A	ENSP00000445008.2:n.-21+1391T>A
ENST00000542344.5:c.-58+1391T>A	ENSP00000444759.1:n.-58+1391T>A
ENST00000544816.5:c.-344+1391T>A	ENSP00000437507.1:n.-344+1391T>A
ENST00000547479.5:c.-21+1391T>A	ENSP00000449333.1:n.-21+1391T>A
ENST00000547704.5:c.-21+1391T>A	ENSP00000446756.1:n.-21+1391T>A
ENST00000547773.5:c.-21+1391T>A	ENSP00000448167.1:n.-21+1391T>A
ENST00000548044.5:c.-107+1391T>A	ENSP00000449649.1:n.-107+1391T>A
ENST00000548273.5:c.-21+1391T>A	ENSP00000446787.1:n.-21+1391T>A
ENST00000549479.1:n.119+1391T>A
ENST00000549596.5:c.-21+1391T>A	ENSP00000447793.1:n.-21+1391T>A
ENST00000549988.5:n.119+1391T>A
ENST00000550934.5:c.-21+1391T>A	ENSP00000448133.1:n.-21+1391T>A
ENST00000551500.1:n.117+1391T>A
ENST00000551600.5:c.-21+1391T>A	ENSP00000448836.1:n.-21+1391T>A
ENST00000551992.5:c.-21+657T>A	ENSP00000448764.1:n.-21+657T>A
ENST00000552342.5:c.-21+1391T>A	ENSP00000447196.1:n.-21+1391T>A
ENST00000618691.4:c.-21+1391T>A	ENSP00000477538.1:n.-21+1391T>A
NM_001307924.1:c.-21+1391T>A	NP_001294853.1:n.-21+1391T>A
NM_004537.4:c.-21+1391T>A	NP_004528.1:n.-21+1391T>A
NM_004537.5:c.-21+1391T>A	NP_004528.1:n.-21+1391T>A
NM_139207.2:c.-21+1391T>A	NP_631946.1:n.-21+1391T>A
NM_139207.3:c.-21+1391T>A	NP_631946.1:n.-21+1391T>A
XM_006719423.2:c.-21+1391T>A	XP_006719486.1:n.-21+1391T>A
XM_006719424.2:c.-21+1391T>A	XP_006719487.1:n.-21+1391T>A
XM_006719425.2:c.-21+1391T>A	XP_006719488.1:n.-21+1391T>A
XM_011538391.1:c.-21+657T>A	XP_011536693.1:n.-21+657T>A
XM_011538392.1:c.-21+1391T>A	XP_011536694.1:n.-21+1391T>A
XM_011538393.1:c.-21+657T>A	XP_011536695.1:n.-21+657T>A
XM_011538395.1:c.-21+657T>A	XP_011536697.1:n.-21+657T>A
NM_001307924.2:c.-21+1391T>A	NP_001294853.1:n.-21+1391T>A
NM_001330231.1:c.-21+1391T>A	NP_001317160.1:n.-21+1391T>A
NM_001330232.1:c.-21+1391T>A	NP_001317161.1:n.-21+1391T>A
NM_004537.6:c.-21+1391T>A	NP_004528.1:n.-21+1391T>A
NM_139207.4:c.-21+1391T>A	NP_631946.1:n.-21+1391T>A
XM_011538393.2:c.-21+657T>A	XP_011536695.1:n.-21+657T>A
XM_017019338.1:c.-21+657T>A	XP_016874827.1:n.-21+657T>A
XM_017019339.1:c.-21+657T>A	XP_016874828.1:n.-21+657T>A
XM_017019340.2:c.-21+1391T>A	XP_016874829.1:n.-21+1391T>A
XM_024448983.1:c.-21+1391T>A	XP_024304751.1:n.-21+1391T>A
XR_001748714.2:n.119+1391T>A
XR_001748715.2:n.119+1391T>A
XR_001748716.1:n.379+657T>A
XR_001748717.2:n.121+1391T>A
XR_002957328.1:n.119+1391T>A
NM_004537.7:c.-21+1391T>A MANE Select	NP_004528.1:n.-21+1391T>A
NM_001307924.3:c.-21+1391T>A	NP_001294853.1:n.-21+1391T>A
NM_001330231.2:c.-21+1391T>A	NP_001317160.1:n.-21+1391T>A
NM_001330232.2:c.-21+1391T>A	NP_001317161.1:n.-21+1391T>A
NM_139207.5:c.-21+1391T>A	NP_631946.1:n.-21+1391T>A