Canonical Allele Identifier: CA2173753181

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711132G= , CM000677.2:g.44711132G=	GRCh38
NC_000015.9:g.45003330G= , CM000677.1:g.45003330G=	GRCh37
NC_000015.8:g.42790622G=	NCBI36
NG_012920.1:g.4646G=
NG_012920.2:g.4656G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-366C= MANE Select	ENSP00000508024.1:n.-366C=
ENST00000558573.1:n.185C=
XM_011521338.1:c.-366C=	XP_011519640.1:n.-366C=
XM_011521339.1:c.-247C=	XP_011519641.1:n.-247C=
XM_011521340.1:c.-188C=	XP_011519642.1:n.-188C=
XM_011521343.1:c.-450C=	XP_011519645.1:n.-450C=
XM_011521345.1:c.-421C=	XP_011519647.1:n.-421C=
XM_011521338.3:c.-366C=	XP_011519640.1:n.-366C=
XM_011521339.3:c.-247C=	XP_011519641.1:n.-247C=
XM_011521340.3:c.-188C=	XP_011519642.1:n.-188C=
XM_011521343.3:c.-450C=	XP_011519645.1:n.-450C=
XM_011521345.3:c.-421C=	XP_011519647.1:n.-421C=
NM_001387260.1:c.-76+200C=	NP_001374189.1:n.-76+200C=
NM_001387261.1:c.-188C=	NP_001374190.1:n.-188C=
NM_001387262.1:c.-456C=	NP_001374191.1:n.-456C=
NM_001387263.1:c.-366C= MANE Select	NP_001374192.1:n.-366C=