Canonical Allele Identifier: CA2173753182

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711135T= , CM000677.2:g.44711135T=	GRCh38
NC_000015.9:g.45003333T= , CM000677.1:g.45003333T=	GRCh37
NC_000015.8:g.42790625T=	NCBI36
NG_012920.1:g.4649T=
NG_012920.2:g.4659T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-369A= MANE Select	ENSP00000508024.1:n.-369A=
ENST00000558573.1:n.182A=
XM_011521338.1:c.-369A=	XP_011519640.1:n.-369A=
XM_011521339.1:c.-250A=	XP_011519641.1:n.-250A=
XM_011521340.1:c.-191A=	XP_011519642.1:n.-191A=
XM_011521343.1:c.-453A=	XP_011519645.1:n.-453A=
XM_011521345.1:c.-424A=	XP_011519647.1:n.-424A=
XM_011521338.3:c.-369A=	XP_011519640.1:n.-369A=
XM_011521339.3:c.-250A=	XP_011519641.1:n.-250A=
XM_011521340.3:c.-191A=	XP_011519642.1:n.-191A=
XM_011521343.3:c.-453A=	XP_011519645.1:n.-453A=
XM_011521345.3:c.-424A=	XP_011519647.1:n.-424A=
NM_001387260.1:c.-76+197A=	NP_001374189.1:n.-76+197A=
NM_001387261.1:c.-191A=	NP_001374190.1:n.-191A=
NM_001387262.1:c.-459A=	NP_001374191.1:n.-459A=
NM_001387263.1:c.-369A= MANE Select	NP_001374192.1:n.-369A=