Canonical Allele Identifier: CA2173753221

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711268G= , CM000677.2:g.44711268G=	GRCh38
NC_000015.9:g.45003466G= , CM000677.1:g.45003466G=	GRCh37
NC_000015.8:g.42790758G=	NCBI36
NG_012920.1:g.4782G=
NG_012920.2:g.4792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-502C= MANE Select	ENSP00000508024.1:n.-502C=
ENST00000558573.1:n.49C=
XM_011521338.1:c.-502C=	XP_011519640.1:n.-502C=
XM_011521339.1:c.-383C=	XP_011519641.1:n.-383C=
XM_011521340.1:c.-324C=	XP_011519642.1:n.-324C=
XM_011521343.1:c.-586C=	XP_011519645.1:n.-586C=
XM_011521345.1:c.-557C=	XP_011519647.1:n.-557C=
XM_011521338.3:c.-502C=	XP_011519640.1:n.-502C=
XM_011521339.3:c.-383C=	XP_011519641.1:n.-383C=
XM_011521340.3:c.-324C=	XP_011519642.1:n.-324C=
XM_011521343.3:c.-586C=	XP_011519645.1:n.-586C=
XM_011521345.3:c.-557C=	XP_011519647.1:n.-557C=
NM_001387260.1:c.-76+64C=	NP_001374189.1:n.-76+64C=
NM_001387261.1:c.-324C=	NP_001374190.1:n.-324C=
NM_001387262.1:c.-592C=	NP_001374191.1:n.-592C=
NM_001387263.1:c.-502C= MANE Select	NP_001374192.1:n.-502C=