Canonical Allele Identifier: CA2628213869

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711107-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711109del , CM000677.2:g.44711109del	GRCh38
NC_000015.9:g.45003307del , CM000677.1:g.45003307del	GRCh37
NC_000015.8:g.42790599del	NCBI36
NG_012920.1:g.4623del
NG_012920.2:g.4633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-342del MANE Select	ENSP00000508024.1:n.-342del
ENST00000558573.1:n.209del
XM_011521338.1:c.-342del	XP_011519640.1:n.-342del
XM_011521339.1:c.-223del	XP_011519641.1:n.-223del
XM_011521340.1:c.-164del	XP_011519642.1:n.-164del
XM_011521343.1:c.-426del	XP_011519645.1:n.-426del
XM_011521345.1:c.-397del	XP_011519647.1:n.-397del
XM_011521338.3:c.-342del	XP_011519640.1:n.-342del
XM_011521339.3:c.-223del	XP_011519641.1:n.-223del
XM_011521340.3:c.-164del	XP_011519642.1:n.-164del
XM_011521343.3:c.-426del	XP_011519645.1:n.-426del
XM_011521345.3:c.-397del	XP_011519647.1:n.-397del
NM_001387260.1:c.-76+224del	NP_001374189.1:n.-76+224del
NM_001387261.1:c.-164del	NP_001374190.1:n.-164del
NM_001387262.1:c.-432del	NP_001374191.1:n.-432del
NM_001387263.1:c.-342del MANE Select	NP_001374192.1:n.-342del