Canonical Allele Identifier: CA2173753209

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711220G= , CM000677.2:g.44711220G=	GRCh38
NC_000015.9:g.45003418G= , CM000677.1:g.45003418G=	GRCh37
NC_000015.8:g.42790710G=	NCBI36
NG_012920.1:g.4734G=
NG_012920.2:g.4744G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-454C= MANE Select	ENSP00000508024.1:n.-454C=
ENST00000558573.1:n.97C=
XM_011521338.1:c.-454C=	XP_011519640.1:n.-454C=
XM_011521339.1:c.-335C=	XP_011519641.1:n.-335C=
XM_011521340.1:c.-276C=	XP_011519642.1:n.-276C=
XM_011521343.1:c.-538C=	XP_011519645.1:n.-538C=
XM_011521345.1:c.-509C=	XP_011519647.1:n.-509C=
XM_011521338.3:c.-454C=	XP_011519640.1:n.-454C=
XM_011521339.3:c.-335C=	XP_011519641.1:n.-335C=
XM_011521340.3:c.-276C=	XP_011519642.1:n.-276C=
XM_011521343.3:c.-538C=	XP_011519645.1:n.-538C=
XM_011521345.3:c.-509C=	XP_011519647.1:n.-509C=
NM_001387260.1:c.-76+112C=	NP_001374189.1:n.-76+112C=
NM_001387261.1:c.-276C=	NP_001374190.1:n.-276C=
NM_001387262.1:c.-544C=	NP_001374191.1:n.-544C=
NM_001387263.1:c.-454C= MANE Select	NP_001374192.1:n.-454C=