Canonical Allele Identifier: CA2173753171

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711092A= , CM000677.2:g.44711092A=	GRCh38
NC_000015.9:g.45003290A= , CM000677.1:g.45003290A=	GRCh37
NC_000015.8:g.42790582A=	NCBI36
NG_012920.1:g.4606A=
NG_012920.2:g.4616A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-326T= MANE Select	ENSP00000508024.1:n.-326T=
ENST00000558573.1:n.225T=
XM_011521338.1:c.-326T=	XP_011519640.1:n.-326T=
XM_011521339.1:c.-207T=	XP_011519641.1:n.-207T=
XM_011521340.1:c.-148T=	XP_011519642.1:n.-148T=
XM_011521343.1:c.-410T=	XP_011519645.1:n.-410T=
XM_011521345.1:c.-381T=	XP_011519647.1:n.-381T=
XM_011521338.3:c.-326T=	XP_011519640.1:n.-326T=
XM_011521339.3:c.-207T=	XP_011519641.1:n.-207T=
XM_011521340.3:c.-148T=	XP_011519642.1:n.-148T=
XM_011521343.3:c.-410T=	XP_011519645.1:n.-410T=
XM_011521345.3:c.-381T=	XP_011519647.1:n.-381T=
NM_001387260.1:c.-76+240T=	NP_001374189.1:n.-76+240T=
NM_001387261.1:c.-148T=	NP_001374190.1:n.-148T=
NM_001387262.1:c.-416T=	NP_001374191.1:n.-416T=
NM_001387263.1:c.-326T= MANE Select	NP_001374192.1:n.-326T=