Canonical Allele Identifier: CA2533552233

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711145del , CM000677.2:g.44711145del	GRCh38
NC_000015.9:g.45003343del , CM000677.1:g.45003343del	GRCh37
NC_000015.8:g.42790635del	NCBI36
NG_012920.1:g.4659del
NG_012920.2:g.4669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-379del MANE Select	ENSP00000508024.1:n.-379del
ENST00000558573.1:n.172del
XM_011521338.1:c.-379del	XP_011519640.1:n.-379del
XM_011521339.1:c.-260del	XP_011519641.1:n.-260del
XM_011521340.1:c.-201del	XP_011519642.1:n.-201del
XM_011521343.1:c.-463del	XP_011519645.1:n.-463del
XM_011521345.1:c.-434del	XP_011519647.1:n.-434del
XM_011521338.3:c.-379del	XP_011519640.1:n.-379del
XM_011521339.3:c.-260del	XP_011519641.1:n.-260del
XM_011521340.3:c.-201del	XP_011519642.1:n.-201del
XM_011521343.3:c.-463del	XP_011519645.1:n.-463del
XM_011521345.3:c.-434del	XP_011519647.1:n.-434del
NM_001387260.1:c.-76+187del	NP_001374189.1:n.-76+187del
NM_001387261.1:c.-201del	NP_001374190.1:n.-201del
NM_001387262.1:c.-469del	NP_001374191.1:n.-469del
NM_001387263.1:c.-379del MANE Select	NP_001374192.1:n.-379del