Canonical Allele Identifier: CA2628214289

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711280-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711284del , CM000677.2:g.44711284del	GRCh38
NC_000015.9:g.45003482del , CM000677.1:g.45003482del	GRCh37
NC_000015.8:g.42790774del	NCBI36
NG_012920.1:g.4798del
NG_012920.2:g.4808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-515del MANE Select	ENSP00000508024.1:n.-515del
ENST00000558573.1:n.36del
XM_011521338.1:c.-515del	XP_011519640.1:n.-515del
XM_011521339.1:c.-396del	XP_011519641.1:n.-396del
XM_011521340.1:c.-337del	XP_011519642.1:n.-337del
XM_011521343.1:c.-599del	XP_011519645.1:n.-599del
XM_011521345.1:c.-570del	XP_011519647.1:n.-570del
XM_011521338.3:c.-515del	XP_011519640.1:n.-515del
XM_011521339.3:c.-396del	XP_011519641.1:n.-396del
XM_011521340.3:c.-337del	XP_011519642.1:n.-337del
XM_011521343.3:c.-599del	XP_011519645.1:n.-599del
XM_011521345.3:c.-570del	XP_011519647.1:n.-570del
NM_001387260.1:c.-76+51del	NP_001374189.1:n.-76+51del
NM_001387261.1:c.-337del	NP_001374190.1:n.-337del
NM_001387262.1:c.-605del	NP_001374191.1:n.-605del
NM_001387263.1:c.-515del MANE Select	NP_001374192.1:n.-515del