Canonical Allele Identifier: CA2173753158

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711039T= , CM000677.2:g.44711039T=	GRCh38
NC_000015.9:g.45003237T= , CM000677.1:g.45003237T=	GRCh37
NC_000015.8:g.42790529T=	NCBI36
NG_012920.1:g.4553T=
NG_012920.2:g.4563T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-273A= MANE Select	ENSP00000508024.1:n.-273A=
ENST00000558573.1:n.278A=
XM_011521338.1:c.-273A=	XP_011519640.1:n.-273A=
XM_011521339.1:c.-154A=	XP_011519641.1:n.-154A=
XM_011521340.1:c.-95A=	XP_011519642.1:n.-95A=
XM_011521343.1:c.-357A=	XP_011519645.1:n.-357A=
XM_011521345.1:c.-328A=	XP_011519647.1:n.-328A=
XM_011521338.3:c.-273A=	XP_011519640.1:n.-273A=
XM_011521339.3:c.-154A=	XP_011519641.1:n.-154A=
XM_011521340.3:c.-95A=	XP_011519642.1:n.-95A=
XM_011521343.3:c.-357A=	XP_011519645.1:n.-357A=
XM_011521345.3:c.-328A=	XP_011519647.1:n.-328A=
NM_001387260.1:c.-76+293A=	NP_001374189.1:n.-76+293A=
NM_001387261.1:c.-95A=	NP_001374190.1:n.-95A=
NM_001387262.1:c.-363A=	NP_001374191.1:n.-363A=
NM_001387263.1:c.-273A= MANE Select	NP_001374192.1:n.-273A=