Canonical Allele Identifier: CA2173753197

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711179G= , CM000677.2:g.44711179G=	GRCh38
NC_000015.9:g.45003377G= , CM000677.1:g.45003377G=	GRCh37
NC_000015.8:g.42790669G=	NCBI36
NG_012920.1:g.4693G=
NG_012920.2:g.4703G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-413C= MANE Select	ENSP00000508024.1:n.-413C=
ENST00000558573.1:n.138C=
XM_011521338.1:c.-413C=	XP_011519640.1:n.-413C=
XM_011521339.1:c.-294C=	XP_011519641.1:n.-294C=
XM_011521340.1:c.-235C=	XP_011519642.1:n.-235C=
XM_011521343.1:c.-497C=	XP_011519645.1:n.-497C=
XM_011521345.1:c.-468C=	XP_011519647.1:n.-468C=
XM_011521338.3:c.-413C=	XP_011519640.1:n.-413C=
XM_011521339.3:c.-294C=	XP_011519641.1:n.-294C=
XM_011521340.3:c.-235C=	XP_011519642.1:n.-235C=
XM_011521343.3:c.-497C=	XP_011519645.1:n.-497C=
XM_011521345.3:c.-468C=	XP_011519647.1:n.-468C=
NM_001387260.1:c.-76+153C=	NP_001374189.1:n.-76+153C=
NM_001387261.1:c.-235C=	NP_001374190.1:n.-235C=
NM_001387262.1:c.-503C=	NP_001374191.1:n.-503C=
NM_001387263.1:c.-413C= MANE Select	NP_001374192.1:n.-413C=