Canonical Allele Identifier: CA2173753230

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711300G= , CM000677.2:g.44711300G=	GRCh38
NC_000015.9:g.45003498G= , CM000677.1:g.45003498G=	GRCh37
NC_000015.8:g.42790790G=	NCBI36
NG_012920.1:g.4814G=
NG_012920.2:g.4824G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-534C= MANE Select	ENSP00000508024.1:n.-534C=
ENST00000558573.1:n.17C=
XM_011521338.1:c.-534C=	XP_011519640.1:n.-534C=
XM_011521339.1:c.-415C=	XP_011519641.1:n.-415C=
XM_011521340.1:c.-356C=	XP_011519642.1:n.-356C=
XM_011521343.1:c.-618C=	XP_011519645.1:n.-618C=
XM_011521345.1:c.-589C=	XP_011519647.1:n.-589C=
XM_011521338.3:c.-534C=	XP_011519640.1:n.-534C=
XM_011521339.3:c.-415C=	XP_011519641.1:n.-415C=
XM_011521340.3:c.-356C=	XP_011519642.1:n.-356C=
XM_011521343.3:c.-618C=	XP_011519645.1:n.-618C=
XM_011521345.3:c.-589C=	XP_011519647.1:n.-589C=
NM_001387260.1:c.-76+32C=	NP_001374189.1:n.-76+32C=
NM_001387261.1:c.-356C=	NP_001374190.1:n.-356C=
NM_001387262.1:c.-624C=	NP_001374191.1:n.-624C=
NM_001387263.1:c.-534C= MANE Select	NP_001374192.1:n.-534C=