Canonical Allele Identifier: CA2628214292

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711316-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711317dup , CM000677.2:g.44711317dup	GRCh38
NC_000015.9:g.45003515dup , CM000677.1:g.45003515dup	GRCh37
NC_000015.8:g.42790807dup	NCBI36
NG_012920.1:g.4831dup
NG_012920.2:g.4841dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-551dup MANE Select	ENSP00000508024.1:n.-551dup
XM_011521338.1:c.-551dup	XP_011519640.1:n.-551dup
XM_011521339.1:c.-432dup	XP_011519641.1:n.-432dup
XM_011521340.1:c.-373dup	XP_011519642.1:n.-373dup
XM_011521343.1:c.-635dup	XP_011519645.1:n.-635dup
XM_011521345.1:c.-606dup	XP_011519647.1:n.-606dup
XM_011521338.3:c.-551dup	XP_011519640.1:n.-551dup
XM_011521339.3:c.-432dup	XP_011519641.1:n.-432dup
XM_011521340.3:c.-373dup	XP_011519642.1:n.-373dup
XM_011521343.3:c.-635dup	XP_011519645.1:n.-635dup
XM_011521345.3:c.-606dup	XP_011519647.1:n.-606dup
NM_001387260.1:c.-76+15dup	NP_001374189.1:n.-76+15dup
NM_001387261.1:c.-373dup	NP_001374190.1:n.-373dup
NM_001387262.1:c.-641dup	NP_001374191.1:n.-641dup
NM_001387263.1:c.-551dup MANE Select	NP_001374192.1:n.-551dup