Canonical Allele Identifier: CA2173753175

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711105C= , CM000677.2:g.44711105C=	GRCh38
NC_000015.9:g.45003303C= , CM000677.1:g.45003303C=	GRCh37
NC_000015.8:g.42790595C=	NCBI36
NG_012920.1:g.4619C=
NG_012920.2:g.4629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-339G= MANE Select	ENSP00000508024.1:n.-339G=
ENST00000558573.1:n.212G=
XM_011521338.1:c.-339G=	XP_011519640.1:n.-339G=
XM_011521339.1:c.-220G=	XP_011519641.1:n.-220G=
XM_011521340.1:c.-161G=	XP_011519642.1:n.-161G=
XM_011521343.1:c.-423G=	XP_011519645.1:n.-423G=
XM_011521345.1:c.-394G=	XP_011519647.1:n.-394G=
XM_011521338.3:c.-339G=	XP_011519640.1:n.-339G=
XM_011521339.3:c.-220G=	XP_011519641.1:n.-220G=
XM_011521340.3:c.-161G=	XP_011519642.1:n.-161G=
XM_011521343.3:c.-423G=	XP_011519645.1:n.-423G=
XM_011521345.3:c.-394G=	XP_011519647.1:n.-394G=
NM_001387260.1:c.-76+227G=	NP_001374189.1:n.-76+227G=
NM_001387261.1:c.-161G=	NP_001374190.1:n.-161G=
NM_001387262.1:c.-429G=	NP_001374191.1:n.-429G=
NM_001387263.1:c.-339G= MANE Select	NP_001374192.1:n.-339G=