Canonical Allele Identifier: CA2173753178

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711115T= , CM000677.2:g.44711115T=	GRCh38
NC_000015.9:g.45003313T= , CM000677.1:g.45003313T=	GRCh37
NC_000015.8:g.42790605T=	NCBI36
NG_012920.1:g.4629T=
NG_012920.2:g.4639T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-349A= MANE Select	ENSP00000508024.1:n.-349A=
ENST00000558573.1:n.202A=
XM_011521338.1:c.-349A=	XP_011519640.1:n.-349A=
XM_011521339.1:c.-230A=	XP_011519641.1:n.-230A=
XM_011521340.1:c.-171A=	XP_011519642.1:n.-171A=
XM_011521343.1:c.-433A=	XP_011519645.1:n.-433A=
XM_011521345.1:c.-404A=	XP_011519647.1:n.-404A=
XM_011521338.3:c.-349A=	XP_011519640.1:n.-349A=
XM_011521339.3:c.-230A=	XP_011519641.1:n.-230A=
XM_011521340.3:c.-171A=	XP_011519642.1:n.-171A=
XM_011521343.3:c.-433A=	XP_011519645.1:n.-433A=
XM_011521345.3:c.-404A=	XP_011519647.1:n.-404A=
NM_001387260.1:c.-76+217A=	NP_001374189.1:n.-76+217A=
NM_001387261.1:c.-171A=	NP_001374190.1:n.-171A=
NM_001387262.1:c.-439A=	NP_001374191.1:n.-439A=
NM_001387263.1:c.-349A= MANE Select	NP_001374192.1:n.-349A=