Canonical Allele Identifier: CA2173753228

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711296G= , CM000677.2:g.44711296G=	GRCh38
NC_000015.9:g.45003494G= , CM000677.1:g.45003494G=	GRCh37
NC_000015.8:g.42790786G=	NCBI36
NG_012920.1:g.4810G=
NG_012920.2:g.4820G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-530C= MANE Select	ENSP00000508024.1:n.-530C=
ENST00000558573.1:n.21C=
XM_011521338.1:c.-530C=	XP_011519640.1:n.-530C=
XM_011521339.1:c.-411C=	XP_011519641.1:n.-411C=
XM_011521340.1:c.-352C=	XP_011519642.1:n.-352C=
XM_011521343.1:c.-614C=	XP_011519645.1:n.-614C=
XM_011521345.1:c.-585C=	XP_011519647.1:n.-585C=
XM_011521338.3:c.-530C=	XP_011519640.1:n.-530C=
XM_011521339.3:c.-411C=	XP_011519641.1:n.-411C=
XM_011521340.3:c.-352C=	XP_011519642.1:n.-352C=
XM_011521343.3:c.-614C=	XP_011519645.1:n.-614C=
XM_011521345.3:c.-585C=	XP_011519647.1:n.-585C=
NM_001387260.1:c.-76+36C=	NP_001374189.1:n.-76+36C=
NM_001387261.1:c.-352C=	NP_001374190.1:n.-352C=
NM_001387262.1:c.-620C=	NP_001374191.1:n.-620C=
NM_001387263.1:c.-530C= MANE Select	NP_001374192.1:n.-530C=