Canonical Allele Identifier: CA2173753231

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711303G= , CM000677.2:g.44711303G=	GRCh38
NC_000015.9:g.45003501G= , CM000677.1:g.45003501G=	GRCh37
NC_000015.8:g.42790793G=	NCBI36
NG_012920.1:g.4817G=
NG_012920.2:g.4827G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-537C= MANE Select	ENSP00000508024.1:n.-537C=
ENST00000558573.1:n.14C=
XM_011521338.1:c.-537C=	XP_011519640.1:n.-537C=
XM_011521339.1:c.-418C=	XP_011519641.1:n.-418C=
XM_011521340.1:c.-359C=	XP_011519642.1:n.-359C=
XM_011521343.1:c.-621C=	XP_011519645.1:n.-621C=
XM_011521345.1:c.-592C=	XP_011519647.1:n.-592C=
XM_011521338.3:c.-537C=	XP_011519640.1:n.-537C=
XM_011521339.3:c.-418C=	XP_011519641.1:n.-418C=
XM_011521340.3:c.-359C=	XP_011519642.1:n.-359C=
XM_011521343.3:c.-621C=	XP_011519645.1:n.-621C=
XM_011521345.3:c.-592C=	XP_011519647.1:n.-592C=
NM_001387260.1:c.-76+29C=	NP_001374189.1:n.-76+29C=
NM_001387261.1:c.-359C=	NP_001374190.1:n.-359C=
NM_001387262.1:c.-627C=	NP_001374191.1:n.-627C=
NM_001387263.1:c.-537C= MANE Select	NP_001374192.1:n.-537C=