Canonical Allele Identifier: CA2628213906

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711131-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711132del , CM000677.2:g.44711132del	GRCh38
NC_000015.9:g.45003330del , CM000677.1:g.45003330del	GRCh37
NC_000015.8:g.42790622del	NCBI36
NG_012920.1:g.4646del
NG_012920.2:g.4656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-366del MANE Select	ENSP00000508024.1:n.-366del
ENST00000558573.1:n.185del
XM_011521338.1:c.-366del	XP_011519640.1:n.-366del
XM_011521339.1:c.-247del	XP_011519641.1:n.-247del
XM_011521340.1:c.-188del	XP_011519642.1:n.-188del
XM_011521343.1:c.-450del	XP_011519645.1:n.-450del
XM_011521345.1:c.-421del	XP_011519647.1:n.-421del
XM_011521338.3:c.-366del	XP_011519640.1:n.-366del
XM_011521339.3:c.-247del	XP_011519641.1:n.-247del
XM_011521340.3:c.-188del	XP_011519642.1:n.-188del
XM_011521343.3:c.-450del	XP_011519645.1:n.-450del
XM_011521345.3:c.-421del	XP_011519647.1:n.-421del
NM_001387260.1:c.-76+200del	NP_001374189.1:n.-76+200del
NM_001387261.1:c.-188del	NP_001374190.1:n.-188del
NM_001387262.1:c.-456del	NP_001374191.1:n.-456del
NM_001387263.1:c.-366del MANE Select	NP_001374192.1:n.-366del