Canonical Allele Identifier: CA2173753208

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711217G= , CM000677.2:g.44711217G=	GRCh38
NC_000015.9:g.45003415G= , CM000677.1:g.45003415G=	GRCh37
NC_000015.8:g.42790707G=	NCBI36
NG_012920.1:g.4731G=
NG_012920.2:g.4741G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-451C= MANE Select	ENSP00000508024.1:n.-451C=
ENST00000558573.1:n.100C=
XM_011521338.1:c.-451C=	XP_011519640.1:n.-451C=
XM_011521339.1:c.-332C=	XP_011519641.1:n.-332C=
XM_011521340.1:c.-273C=	XP_011519642.1:n.-273C=
XM_011521343.1:c.-535C=	XP_011519645.1:n.-535C=
XM_011521345.1:c.-506C=	XP_011519647.1:n.-506C=
XM_011521338.3:c.-451C=	XP_011519640.1:n.-451C=
XM_011521339.3:c.-332C=	XP_011519641.1:n.-332C=
XM_011521340.3:c.-273C=	XP_011519642.1:n.-273C=
XM_011521343.3:c.-535C=	XP_011519645.1:n.-535C=
XM_011521345.3:c.-506C=	XP_011519647.1:n.-506C=
NM_001387260.1:c.-76+115C=	NP_001374189.1:n.-76+115C=
NM_001387261.1:c.-273C=	NP_001374190.1:n.-273C=
NM_001387262.1:c.-541C=	NP_001374191.1:n.-541C=
NM_001387263.1:c.-451C= MANE Select	NP_001374192.1:n.-451C=