Canonical Allele Identifier: CA2173753211

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711230T= , CM000677.2:g.44711230T=	GRCh38
NC_000015.9:g.45003428T= , CM000677.1:g.45003428T=	GRCh37
NC_000015.8:g.42790720T=	NCBI36
NG_012920.1:g.4744T=
NG_012920.2:g.4754T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-464A= MANE Select	ENSP00000508024.1:n.-464A=
ENST00000558573.1:n.87A=
XM_011521338.1:c.-464A=	XP_011519640.1:n.-464A=
XM_011521339.1:c.-345A=	XP_011519641.1:n.-345A=
XM_011521340.1:c.-286A=	XP_011519642.1:n.-286A=
XM_011521343.1:c.-548A=	XP_011519645.1:n.-548A=
XM_011521345.1:c.-519A=	XP_011519647.1:n.-519A=
XM_011521338.3:c.-464A=	XP_011519640.1:n.-464A=
XM_011521339.3:c.-345A=	XP_011519641.1:n.-345A=
XM_011521340.3:c.-286A=	XP_011519642.1:n.-286A=
XM_011521343.3:c.-548A=	XP_011519645.1:n.-548A=
XM_011521345.3:c.-519A=	XP_011519647.1:n.-519A=
NM_001387260.1:c.-76+102A=	NP_001374189.1:n.-76+102A=
NM_001387261.1:c.-286A=	NP_001374190.1:n.-286A=
NM_001387262.1:c.-554A=	NP_001374191.1:n.-554A=
NM_001387263.1:c.-464A= MANE Select	NP_001374192.1:n.-464A=