Canonical Allele Identifier: CA2173753210

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711223G= , CM000677.2:g.44711223G=	GRCh38
NC_000015.9:g.45003421G= , CM000677.1:g.45003421G=	GRCh37
NC_000015.8:g.42790713G=	NCBI36
NG_012920.1:g.4737G=
NG_012920.2:g.4747G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-457C= MANE Select	ENSP00000508024.1:n.-457C=
ENST00000558573.1:n.94C=
XM_011521338.1:c.-457C=	XP_011519640.1:n.-457C=
XM_011521339.1:c.-338C=	XP_011519641.1:n.-338C=
XM_011521340.1:c.-279C=	XP_011519642.1:n.-279C=
XM_011521343.1:c.-541C=	XP_011519645.1:n.-541C=
XM_011521345.1:c.-512C=	XP_011519647.1:n.-512C=
XM_011521338.3:c.-457C=	XP_011519640.1:n.-457C=
XM_011521339.3:c.-338C=	XP_011519641.1:n.-338C=
XM_011521340.3:c.-279C=	XP_011519642.1:n.-279C=
XM_011521343.3:c.-541C=	XP_011519645.1:n.-541C=
XM_011521345.3:c.-512C=	XP_011519647.1:n.-512C=
NM_001387260.1:c.-76+109C=	NP_001374189.1:n.-76+109C=
NM_001387261.1:c.-279C=	NP_001374190.1:n.-279C=
NM_001387262.1:c.-547C=	NP_001374191.1:n.-547C=
NM_001387263.1:c.-457C= MANE Select	NP_001374192.1:n.-457C=