Canonical Allele Identifier: CA2173753240

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711320C= , CM000677.2:g.44711320C=	GRCh38
NC_000015.9:g.45003518C= , CM000677.1:g.45003518C=	GRCh37
NC_000015.8:g.42790810C=	NCBI36
NG_012920.1:g.4834C=
NG_012920.2:g.4844C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-554G= MANE Select	ENSP00000508024.1:n.-554G=
XM_011521338.1:c.-554G=	XP_011519640.1:n.-554G=
XM_011521339.1:c.-435G=	XP_011519641.1:n.-435G=
XM_011521340.1:c.-376G=	XP_011519642.1:n.-376G=
XM_011521343.1:c.-638G=	XP_011519645.1:n.-638G=
XM_011521345.1:c.-609G=	XP_011519647.1:n.-609G=
XM_011521338.3:c.-554G=	XP_011519640.1:n.-554G=
XM_011521339.3:c.-435G=	XP_011519641.1:n.-435G=
XM_011521340.3:c.-376G=	XP_011519642.1:n.-376G=
XM_011521343.3:c.-638G=	XP_011519645.1:n.-638G=
XM_011521345.3:c.-609G=	XP_011519647.1:n.-609G=
NM_001387260.1:c.-76+12G=	NP_001374189.1:n.-76+12G=
NM_001387261.1:c.-376G=	NP_001374190.1:n.-376G=
NM_001387262.1:c.-644G=	NP_001374191.1:n.-644G=
NM_001387263.1:c.-554G= MANE Select	NP_001374192.1:n.-554G=