Canonical Allele Identifier: CA2173753188

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711159A= , CM000677.2:g.44711159A=	GRCh38
NC_000015.9:g.45003357A= , CM000677.1:g.45003357A=	GRCh37
NC_000015.8:g.42790649A=	NCBI36
NG_012920.1:g.4673A=
NG_012920.2:g.4683A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-393T= MANE Select	ENSP00000508024.1:n.-393T=
ENST00000558573.1:n.158T=
XM_011521338.1:c.-393T=	XP_011519640.1:n.-393T=
XM_011521339.1:c.-274T=	XP_011519641.1:n.-274T=
XM_011521340.1:c.-215T=	XP_011519642.1:n.-215T=
XM_011521343.1:c.-477T=	XP_011519645.1:n.-477T=
XM_011521345.1:c.-448T=	XP_011519647.1:n.-448T=
XM_011521338.3:c.-393T=	XP_011519640.1:n.-393T=
XM_011521339.3:c.-274T=	XP_011519641.1:n.-274T=
XM_011521340.3:c.-215T=	XP_011519642.1:n.-215T=
XM_011521343.3:c.-477T=	XP_011519645.1:n.-477T=
XM_011521345.3:c.-448T=	XP_011519647.1:n.-448T=
NM_001387260.1:c.-76+173T=	NP_001374189.1:n.-76+173T=
NM_001387261.1:c.-215T=	NP_001374190.1:n.-215T=
NM_001387262.1:c.-483T=	NP_001374191.1:n.-483T=
NM_001387263.1:c.-393T= MANE Select	NP_001374192.1:n.-393T=