Canonical Allele Identifier: CA2173753179

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711121T= , CM000677.2:g.44711121T=	GRCh38
NC_000015.9:g.45003319T= , CM000677.1:g.45003319T=	GRCh37
NC_000015.8:g.42790611T=	NCBI36
NG_012920.1:g.4635T=
NG_012920.2:g.4645T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-355A= MANE Select	ENSP00000508024.1:n.-355A=
ENST00000558573.1:n.196A=
XM_011521338.1:c.-355A=	XP_011519640.1:n.-355A=
XM_011521339.1:c.-236A=	XP_011519641.1:n.-236A=
XM_011521340.1:c.-177A=	XP_011519642.1:n.-177A=
XM_011521343.1:c.-439A=	XP_011519645.1:n.-439A=
XM_011521345.1:c.-410A=	XP_011519647.1:n.-410A=
XM_011521338.3:c.-355A=	XP_011519640.1:n.-355A=
XM_011521339.3:c.-236A=	XP_011519641.1:n.-236A=
XM_011521340.3:c.-177A=	XP_011519642.1:n.-177A=
XM_011521343.3:c.-439A=	XP_011519645.1:n.-439A=
XM_011521345.3:c.-410A=	XP_011519647.1:n.-410A=
NM_001387260.1:c.-76+211A=	NP_001374189.1:n.-76+211A=
NM_001387261.1:c.-177A=	NP_001374190.1:n.-177A=
NM_001387262.1:c.-445A=	NP_001374191.1:n.-445A=
NM_001387263.1:c.-355A= MANE Select	NP_001374192.1:n.-355A=