Canonical Allele Identifier: CA2173753184

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711150C= , CM000677.2:g.44711150C=	GRCh38
NC_000015.9:g.45003348C= , CM000677.1:g.45003348C=	GRCh37
NC_000015.8:g.42790640C=	NCBI36
NG_012920.1:g.4664C=
NG_012920.2:g.4674C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-384G= MANE Select	ENSP00000508024.1:n.-384G=
ENST00000558573.1:n.167G=
XM_011521338.1:c.-384G=	XP_011519640.1:n.-384G=
XM_011521339.1:c.-265G=	XP_011519641.1:n.-265G=
XM_011521340.1:c.-206G=	XP_011519642.1:n.-206G=
XM_011521343.1:c.-468G=	XP_011519645.1:n.-468G=
XM_011521345.1:c.-439G=	XP_011519647.1:n.-439G=
XM_011521338.3:c.-384G=	XP_011519640.1:n.-384G=
XM_011521339.3:c.-265G=	XP_011519641.1:n.-265G=
XM_011521340.3:c.-206G=	XP_011519642.1:n.-206G=
XM_011521343.3:c.-468G=	XP_011519645.1:n.-468G=
XM_011521345.3:c.-439G=	XP_011519647.1:n.-439G=
NM_001387260.1:c.-76+182G=	NP_001374189.1:n.-76+182G=
NM_001387261.1:c.-206G=	NP_001374190.1:n.-206G=
NM_001387262.1:c.-474G=	NP_001374191.1:n.-474G=
NM_001387263.1:c.-384G= MANE Select	NP_001374192.1:n.-384G=