Canonical Allele Identifier: CA2173753222

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711277A= , CM000677.2:g.44711277A=	GRCh38
NC_000015.9:g.45003475A= , CM000677.1:g.45003475A=	GRCh37
NC_000015.8:g.42790767A=	NCBI36
NG_012920.1:g.4791A=
NG_012920.2:g.4801A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-511T= MANE Select	ENSP00000508024.1:n.-511T=
ENST00000558573.1:n.40T=
XM_011521338.1:c.-511T=	XP_011519640.1:n.-511T=
XM_011521339.1:c.-392T=	XP_011519641.1:n.-392T=
XM_011521340.1:c.-333T=	XP_011519642.1:n.-333T=
XM_011521343.1:c.-595T=	XP_011519645.1:n.-595T=
XM_011521345.1:c.-566T=	XP_011519647.1:n.-566T=
XM_011521338.3:c.-511T=	XP_011519640.1:n.-511T=
XM_011521339.3:c.-392T=	XP_011519641.1:n.-392T=
XM_011521340.3:c.-333T=	XP_011519642.1:n.-333T=
XM_011521343.3:c.-595T=	XP_011519645.1:n.-595T=
XM_011521345.3:c.-566T=	XP_011519647.1:n.-566T=
NM_001387260.1:c.-76+55T=	NP_001374189.1:n.-76+55T=
NM_001387261.1:c.-333T=	NP_001374190.1:n.-333T=
NM_001387262.1:c.-601T=	NP_001374191.1:n.-601T=
NM_001387263.1:c.-511T= MANE Select	NP_001374192.1:n.-511T=