Canonical Allele Identifier: CA2173753235

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711312T= , CM000677.2:g.44711312T=	GRCh38
NC_000015.9:g.45003510T= , CM000677.1:g.45003510T=	GRCh37
NC_000015.8:g.42790802T=	NCBI36
NG_012920.1:g.4826T=
NG_012920.2:g.4836T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-546A= MANE Select	ENSP00000508024.1:n.-546A=
ENST00000558573.1:n.5A=
XM_011521338.1:c.-546A=	XP_011519640.1:n.-546A=
XM_011521339.1:c.-427A=	XP_011519641.1:n.-427A=
XM_011521340.1:c.-368A=	XP_011519642.1:n.-368A=
XM_011521343.1:c.-630A=	XP_011519645.1:n.-630A=
XM_011521345.1:c.-601A=	XP_011519647.1:n.-601A=
XM_011521338.3:c.-546A=	XP_011519640.1:n.-546A=
XM_011521339.3:c.-427A=	XP_011519641.1:n.-427A=
XM_011521340.3:c.-368A=	XP_011519642.1:n.-368A=
XM_011521343.3:c.-630A=	XP_011519645.1:n.-630A=
XM_011521345.3:c.-601A=	XP_011519647.1:n.-601A=
NM_001387260.1:c.-76+20A=	NP_001374189.1:n.-76+20A=
NM_001387261.1:c.-368A=	NP_001374190.1:n.-368A=
NM_001387262.1:c.-636A=	NP_001374191.1:n.-636A=
NM_001387263.1:c.-546A= MANE Select	NP_001374192.1:n.-546A=