Canonical Allele Identifier: CA2173753232

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711305G= , CM000677.2:g.44711305G=	GRCh38
NC_000015.9:g.45003503G= , CM000677.1:g.45003503G=	GRCh37
NC_000015.8:g.42790795G=	NCBI36
NG_012920.1:g.4819G=
NG_012920.2:g.4829G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-539C= MANE Select	ENSP00000508024.1:n.-539C=
ENST00000558573.1:n.12C=
XM_011521338.1:c.-539C=	XP_011519640.1:n.-539C=
XM_011521339.1:c.-420C=	XP_011519641.1:n.-420C=
XM_011521340.1:c.-361C=	XP_011519642.1:n.-361C=
XM_011521343.1:c.-623C=	XP_011519645.1:n.-623C=
XM_011521345.1:c.-594C=	XP_011519647.1:n.-594C=
XM_011521338.3:c.-539C=	XP_011519640.1:n.-539C=
XM_011521339.3:c.-420C=	XP_011519641.1:n.-420C=
XM_011521340.3:c.-361C=	XP_011519642.1:n.-361C=
XM_011521343.3:c.-623C=	XP_011519645.1:n.-623C=
XM_011521345.3:c.-594C=	XP_011519647.1:n.-594C=
NM_001387260.1:c.-76+27C=	NP_001374189.1:n.-76+27C=
NM_001387261.1:c.-361C=	NP_001374190.1:n.-361C=
NM_001387262.1:c.-629C=	NP_001374191.1:n.-629C=
NM_001387263.1:c.-539C= MANE Select	NP_001374192.1:n.-539C=