Canonical Allele Identifier: CA2173753260

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711350T= , CM000677.2:g.44711350T=	GRCh38
NC_000015.9:g.45003548T= , CM000677.1:g.45003548T=	GRCh37
NC_000015.8:g.42790840T=	NCBI36
NG_012920.1:g.4864T=
NG_012920.2:g.4874T=

Transcript Alleles

HGVS	Amino-acid change
XM_011521338.1:c.-584A=	XP_011519640.1:n.-584A=
XM_011521339.1:c.-465A=	XP_011519641.1:n.-465A=
XM_011521340.1:c.-406A=	XP_011519642.1:n.-406A=
XM_011521343.1:c.-668A=	XP_011519645.1:n.-668A=
XM_011521345.1:c.-639A=	XP_011519647.1:n.-639A=
XM_011521338.3:c.-584A=	XP_011519640.1:n.-584A=
XM_011521339.3:c.-465A=	XP_011519641.1:n.-465A=
XM_011521340.3:c.-406A=	XP_011519642.1:n.-406A=
XM_011521343.3:c.-668A=	XP_011519645.1:n.-668A=
XM_011521345.3:c.-639A=	XP_011519647.1:n.-639A=
NM_001387260.1:c.-94A=	NP_001374189.1:n.-94A=