Canonical Allele Identifier: CA2628213967

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711158-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711160del , CM000677.2:g.44711160del	GRCh38
NC_000015.9:g.45003358del , CM000677.1:g.45003358del	GRCh37
NC_000015.8:g.42790650del	NCBI36
NG_012920.1:g.4674del
NG_012920.2:g.4684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-393del MANE Select	ENSP00000508024.1:n.-393del
ENST00000558573.1:n.158del
XM_011521338.1:c.-393del	XP_011519640.1:n.-393del
XM_011521339.1:c.-274del	XP_011519641.1:n.-274del
XM_011521340.1:c.-215del	XP_011519642.1:n.-215del
XM_011521343.1:c.-477del	XP_011519645.1:n.-477del
XM_011521345.1:c.-448del	XP_011519647.1:n.-448del
XM_011521338.3:c.-393del	XP_011519640.1:n.-393del
XM_011521339.3:c.-274del	XP_011519641.1:n.-274del
XM_011521340.3:c.-215del	XP_011519642.1:n.-215del
XM_011521343.3:c.-477del	XP_011519645.1:n.-477del
XM_011521345.3:c.-448del	XP_011519647.1:n.-448del
NM_001387260.1:c.-76+173del	NP_001374189.1:n.-76+173del
NM_001387261.1:c.-215del	NP_001374190.1:n.-215del
NM_001387262.1:c.-483del	NP_001374191.1:n.-483del
NM_001387263.1:c.-393del MANE Select	NP_001374192.1:n.-393del