Canonical Allele Identifier: CA2173753159

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711054A= , CM000677.2:g.44711054A=	GRCh38
NC_000015.9:g.45003252A= , CM000677.1:g.45003252A=	GRCh37
NC_000015.8:g.42790544A=	NCBI36
NG_012920.1:g.4568A=
NG_012920.2:g.4578A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-288T= MANE Select	ENSP00000508024.1:n.-288T=
ENST00000558573.1:n.263T=
XM_011521338.1:c.-288T=	XP_011519640.1:n.-288T=
XM_011521339.1:c.-169T=	XP_011519641.1:n.-169T=
XM_011521340.1:c.-110T=	XP_011519642.1:n.-110T=
XM_011521343.1:c.-372T=	XP_011519645.1:n.-372T=
XM_011521345.1:c.-343T=	XP_011519647.1:n.-343T=
XM_011521338.3:c.-288T=	XP_011519640.1:n.-288T=
XM_011521339.3:c.-169T=	XP_011519641.1:n.-169T=
XM_011521340.3:c.-110T=	XP_011519642.1:n.-110T=
XM_011521343.3:c.-372T=	XP_011519645.1:n.-372T=
XM_011521345.3:c.-343T=	XP_011519647.1:n.-343T=
NM_001387260.1:c.-76+278T=	NP_001374189.1:n.-76+278T=
NM_001387261.1:c.-110T=	NP_001374190.1:n.-110T=
NM_001387262.1:c.-378T=	NP_001374191.1:n.-378T=
NM_001387263.1:c.-288T= MANE Select	NP_001374192.1:n.-288T=