Canonical Allele Identifier: CA2173753189

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711162T= , CM000677.2:g.44711162T=	GRCh38
NC_000015.9:g.45003360T= , CM000677.1:g.45003360T=	GRCh37
NC_000015.8:g.42790652T=	NCBI36
NG_012920.1:g.4676T=
NG_012920.2:g.4686T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-396A= MANE Select	ENSP00000508024.1:n.-396A=
ENST00000558573.1:n.155A=
XM_011521338.1:c.-396A=	XP_011519640.1:n.-396A=
XM_011521339.1:c.-277A=	XP_011519641.1:n.-277A=
XM_011521340.1:c.-218A=	XP_011519642.1:n.-218A=
XM_011521343.1:c.-480A=	XP_011519645.1:n.-480A=
XM_011521345.1:c.-451A=	XP_011519647.1:n.-451A=
XM_011521338.3:c.-396A=	XP_011519640.1:n.-396A=
XM_011521339.3:c.-277A=	XP_011519641.1:n.-277A=
XM_011521340.3:c.-218A=	XP_011519642.1:n.-218A=
XM_011521343.3:c.-480A=	XP_011519645.1:n.-480A=
XM_011521345.3:c.-451A=	XP_011519647.1:n.-451A=
NM_001387260.1:c.-76+170A=	NP_001374189.1:n.-76+170A=
NM_001387261.1:c.-218A=	NP_001374190.1:n.-218A=
NM_001387262.1:c.-486A=	NP_001374191.1:n.-486A=
NM_001387263.1:c.-396A= MANE Select	NP_001374192.1:n.-396A=