Canonical Allele Identifier: CA2628213815

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711069-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711070del , CM000677.2:g.44711070del	GRCh38
NC_000015.9:g.45003268del , CM000677.1:g.45003268del	GRCh37
NC_000015.8:g.42790560del	NCBI36
NG_012920.1:g.4584del
NG_012920.2:g.4594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-304del MANE Select	ENSP00000508024.1:n.-304del
ENST00000558573.1:n.247del
XM_011521338.1:c.-304del	XP_011519640.1:n.-304del
XM_011521339.1:c.-185del	XP_011519641.1:n.-185del
XM_011521340.1:c.-126del	XP_011519642.1:n.-126del
XM_011521343.1:c.-388del	XP_011519645.1:n.-388del
XM_011521345.1:c.-359del	XP_011519647.1:n.-359del
XM_011521338.3:c.-304del	XP_011519640.1:n.-304del
XM_011521339.3:c.-185del	XP_011519641.1:n.-185del
XM_011521340.3:c.-126del	XP_011519642.1:n.-126del
XM_011521343.3:c.-388del	XP_011519645.1:n.-388del
XM_011521345.3:c.-359del	XP_011519647.1:n.-359del
NM_001387260.1:c.-76+262del	NP_001374189.1:n.-76+262del
NM_001387261.1:c.-126del	NP_001374190.1:n.-126del
NM_001387262.1:c.-394del	NP_001374191.1:n.-394del
NM_001387263.1:c.-304del MANE Select	NP_001374192.1:n.-304del