Canonical Allele Identifier: CA2803979431

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711165_44711166insG , CM000677.2:g.44711165_44711166insG	GRCh38
NC_000015.9:g.45003363_45003364insG , CM000677.1:g.45003363_45003364insG	GRCh37
NC_000015.8:g.42790655_42790656insG	NCBI36
NG_012920.1:g.4679_4680insG
NG_012920.2:g.4689_4690insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-400_-399insC MANE Select	ENSP00000508024.1:n.-400_-399insC
ENST00000558573.1:n.151_152insC
XM_011521338.1:c.-400_-399insC	XP_011519640.1:n.-400_-399insC
XM_011521339.1:c.-281_-280insC	XP_011519641.1:n.-281_-280insC
XM_011521340.1:c.-222_-221insC	XP_011519642.1:n.-222_-221insC
XM_011521343.1:c.-484_-483insC	XP_011519645.1:n.-484_-483insC
XM_011521345.1:c.-455_-454insC	XP_011519647.1:n.-455_-454insC
XM_011521338.3:c.-400_-399insC	XP_011519640.1:n.-400_-399insC
XM_011521339.3:c.-281_-280insC	XP_011519641.1:n.-281_-280insC
XM_011521340.3:c.-222_-221insC	XP_011519642.1:n.-222_-221insC
XM_011521343.3:c.-484_-483insC	XP_011519645.1:n.-484_-483insC
XM_011521345.3:c.-455_-454insC	XP_011519647.1:n.-455_-454insC
NM_001387260.1:c.-76+166_-76+167insC	NP_001374189.1:n.-76+166_-76+167insC
NM_001387261.1:c.-222_-221insC	NP_001374190.1:n.-222_-221insC
NM_001387262.1:c.-490_-489insC	NP_001374191.1:n.-490_-489insC
NM_001387263.1:c.-400_-399insC MANE Select	NP_001374192.1:n.-400_-399insC