Canonical Allele Identifier: CA2173753223

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711279C= , CM000677.2:g.44711279C=	GRCh38
NC_000015.9:g.45003477C= , CM000677.1:g.45003477C=	GRCh37
NC_000015.8:g.42790769C=	NCBI36
NG_012920.1:g.4793C=
NG_012920.2:g.4803C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-513G= MANE Select	ENSP00000508024.1:n.-513G=
ENST00000558573.1:n.38G=
XM_011521338.1:c.-513G=	XP_011519640.1:n.-513G=
XM_011521339.1:c.-394G=	XP_011519641.1:n.-394G=
XM_011521340.1:c.-335G=	XP_011519642.1:n.-335G=
XM_011521343.1:c.-597G=	XP_011519645.1:n.-597G=
XM_011521345.1:c.-568G=	XP_011519647.1:n.-568G=
XM_011521338.3:c.-513G=	XP_011519640.1:n.-513G=
XM_011521339.3:c.-394G=	XP_011519641.1:n.-394G=
XM_011521340.3:c.-335G=	XP_011519642.1:n.-335G=
XM_011521343.3:c.-597G=	XP_011519645.1:n.-597G=
XM_011521345.3:c.-568G=	XP_011519647.1:n.-568G=
NM_001387260.1:c.-76+53G=	NP_001374189.1:n.-76+53G=
NM_001387261.1:c.-335G=	NP_001374190.1:n.-335G=
NM_001387262.1:c.-603G=	NP_001374191.1:n.-603G=
NM_001387263.1:c.-513G= MANE Select	NP_001374192.1:n.-513G=