Canonical Allele Identifier: CA2173753205

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711205A= , CM000677.2:g.44711205A=	GRCh38
NC_000015.9:g.45003403A= , CM000677.1:g.45003403A=	GRCh37
NC_000015.8:g.42790695A=	NCBI36
NG_012920.1:g.4719A=
NG_012920.2:g.4729A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-439T= MANE Select	ENSP00000508024.1:n.-439T=
ENST00000558573.1:n.112T=
XM_011521338.1:c.-439T=	XP_011519640.1:n.-439T=
XM_011521339.1:c.-320T=	XP_011519641.1:n.-320T=
XM_011521340.1:c.-261T=	XP_011519642.1:n.-261T=
XM_011521343.1:c.-523T=	XP_011519645.1:n.-523T=
XM_011521345.1:c.-494T=	XP_011519647.1:n.-494T=
XM_011521338.3:c.-439T=	XP_011519640.1:n.-439T=
XM_011521339.3:c.-320T=	XP_011519641.1:n.-320T=
XM_011521340.3:c.-261T=	XP_011519642.1:n.-261T=
XM_011521343.3:c.-523T=	XP_011519645.1:n.-523T=
XM_011521345.3:c.-494T=	XP_011519647.1:n.-494T=
NM_001387260.1:c.-76+127T=	NP_001374189.1:n.-76+127T=
NM_001387261.1:c.-261T=	NP_001374190.1:n.-261T=
NM_001387262.1:c.-529T=	NP_001374191.1:n.-529T=
NM_001387263.1:c.-439T= MANE Select	NP_001374192.1:n.-439T=