Canonical Allele Identifier: CA2173753216

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711255A= , CM000677.2:g.44711255A=	GRCh38
NC_000015.9:g.45003453A= , CM000677.1:g.45003453A=	GRCh37
NC_000015.8:g.42790745A=	NCBI36
NG_012920.1:g.4769A=
NG_012920.2:g.4779A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-489T= MANE Select	ENSP00000508024.1:n.-489T=
ENST00000558573.1:n.62T=
XM_011521338.1:c.-489T=	XP_011519640.1:n.-489T=
XM_011521339.1:c.-370T=	XP_011519641.1:n.-370T=
XM_011521340.1:c.-311T=	XP_011519642.1:n.-311T=
XM_011521343.1:c.-573T=	XP_011519645.1:n.-573T=
XM_011521345.1:c.-544T=	XP_011519647.1:n.-544T=
XM_011521338.3:c.-489T=	XP_011519640.1:n.-489T=
XM_011521339.3:c.-370T=	XP_011519641.1:n.-370T=
XM_011521340.3:c.-311T=	XP_011519642.1:n.-311T=
XM_011521343.3:c.-573T=	XP_011519645.1:n.-573T=
XM_011521345.3:c.-544T=	XP_011519647.1:n.-544T=
NM_001387260.1:c.-76+77T=	NP_001374189.1:n.-76+77T=
NM_001387261.1:c.-311T=	NP_001374190.1:n.-311T=
NM_001387262.1:c.-579T=	NP_001374191.1:n.-579T=
NM_001387263.1:c.-489T= MANE Select	NP_001374192.1:n.-489T=