Canonical Allele Identifier: CA2628214282

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711207-T-TCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711209_44711211dup , CM000677.2:g.44711209_44711211dup	GRCh38
NC_000015.9:g.45003407_45003409dup , CM000677.1:g.45003407_45003409dup	GRCh37
NC_000015.8:g.42790699_42790701dup	NCBI36
NG_012920.1:g.4723_4725dup
NG_012920.2:g.4733_4735dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-444_-442dup MANE Select	ENSP00000508024.1:n.-444_-442dup
ENST00000558573.1:n.107_109dup
XM_011521338.1:c.-444_-442dup	XP_011519640.1:n.-444_-442dup
XM_011521339.1:c.-325_-323dup	XP_011519641.1:n.-325_-323dup
XM_011521340.1:c.-266_-264dup	XP_011519642.1:n.-266_-264dup
XM_011521343.1:c.-528_-526dup	XP_011519645.1:n.-528_-526dup
XM_011521345.1:c.-499_-497dup	XP_011519647.1:n.-499_-497dup
XM_011521338.3:c.-444_-442dup	XP_011519640.1:n.-444_-442dup
XM_011521339.3:c.-325_-323dup	XP_011519641.1:n.-325_-323dup
XM_011521340.3:c.-266_-264dup	XP_011519642.1:n.-266_-264dup
XM_011521343.3:c.-528_-526dup	XP_011519645.1:n.-528_-526dup
XM_011521345.3:c.-499_-497dup	XP_011519647.1:n.-499_-497dup
NM_001387260.1:c.-76+122_-76+124dup	NP_001374189.1:n.-76+122_-76+124dup
NM_001387261.1:c.-266_-264dup	NP_001374190.1:n.-266_-264dup
NM_001387262.1:c.-534_-532dup	NP_001374191.1:n.-534_-532dup
NM_001387263.1:c.-444_-442dup MANE Select	NP_001374192.1:n.-444_-442dup