Canonical Allele Identifier: CA2173753166

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711078T= , CM000677.2:g.44711078T=	GRCh38
NC_000015.9:g.45003276T= , CM000677.1:g.45003276T=	GRCh37
NC_000015.8:g.42790568T=	NCBI36
NG_012920.1:g.4592T=
NG_012920.2:g.4602T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-312A= MANE Select	ENSP00000508024.1:n.-312A=
ENST00000558573.1:n.239A=
XM_011521338.1:c.-312A=	XP_011519640.1:n.-312A=
XM_011521339.1:c.-193A=	XP_011519641.1:n.-193A=
XM_011521340.1:c.-134A=	XP_011519642.1:n.-134A=
XM_011521343.1:c.-396A=	XP_011519645.1:n.-396A=
XM_011521345.1:c.-367A=	XP_011519647.1:n.-367A=
XM_011521338.3:c.-312A=	XP_011519640.1:n.-312A=
XM_011521339.3:c.-193A=	XP_011519641.1:n.-193A=
XM_011521340.3:c.-134A=	XP_011519642.1:n.-134A=
XM_011521343.3:c.-396A=	XP_011519645.1:n.-396A=
XM_011521345.3:c.-367A=	XP_011519647.1:n.-367A=
NM_001387260.1:c.-76+254A=	NP_001374189.1:n.-76+254A=
NM_001387261.1:c.-134A=	NP_001374190.1:n.-134A=
NM_001387262.1:c.-402A=	NP_001374191.1:n.-402A=
NM_001387263.1:c.-312A= MANE Select	NP_001374192.1:n.-312A=