Canonical Allele Identifier: CA2173753256

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711341T= , CM000677.2:g.44711341T=	GRCh38
NC_000015.9:g.45003539T= , CM000677.1:g.45003539T=	GRCh37
NC_000015.8:g.42790831T=	NCBI36
NG_012920.1:g.4855T=
NG_012920.2:g.4865T=

Transcript Alleles

HGVS	Amino-acid Change
XM_011521338.1:c.-575A=	XP_011519640.1:n.-575A=
XM_011521339.1:c.-456A=	XP_011519641.1:n.-456A=
XM_011521340.1:c.-397A=	XP_011519642.1:n.-397A=
XM_011521343.1:c.-659A=	XP_011519645.1:n.-659A=
XM_011521345.1:c.-630A=	XP_011519647.1:n.-630A=
XM_011521338.3:c.-575A=	XP_011519640.1:n.-575A=
XM_011521339.3:c.-456A=	XP_011519641.1:n.-456A=
XM_011521340.3:c.-397A=	XP_011519642.1:n.-397A=
XM_011521343.3:c.-659A=	XP_011519645.1:n.-659A=
XM_011521345.3:c.-630A=	XP_011519647.1:n.-630A=
NM_001387260.1:c.-85A=	NP_001374189.1:n.-85A=