Canonical Allele Identifier: CA2173753192

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711166T= , CM000677.2:g.44711166T=	GRCh38
NC_000015.9:g.45003364T= , CM000677.1:g.45003364T=	GRCh37
NC_000015.8:g.42790656T=	NCBI36
NG_012920.1:g.4680T=
NG_012920.2:g.4690T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-400A= MANE Select	ENSP00000508024.1:n.-400A=
ENST00000558573.1:n.151A=
XM_011521338.1:c.-400A=	XP_011519640.1:n.-400A=
XM_011521339.1:c.-281A=	XP_011519641.1:n.-281A=
XM_011521340.1:c.-222A=	XP_011519642.1:n.-222A=
XM_011521343.1:c.-484A=	XP_011519645.1:n.-484A=
XM_011521345.1:c.-455A=	XP_011519647.1:n.-455A=
XM_011521338.3:c.-400A=	XP_011519640.1:n.-400A=
XM_011521339.3:c.-281A=	XP_011519641.1:n.-281A=
XM_011521340.3:c.-222A=	XP_011519642.1:n.-222A=
XM_011521343.3:c.-484A=	XP_011519645.1:n.-484A=
XM_011521345.3:c.-455A=	XP_011519647.1:n.-455A=
NM_001387260.1:c.-76+166A=	NP_001374189.1:n.-76+166A=
NM_001387261.1:c.-222A=	NP_001374190.1:n.-222A=
NM_001387262.1:c.-490A=	NP_001374191.1:n.-490A=
NM_001387263.1:c.-400A= MANE Select	NP_001374192.1:n.-400A=