Canonical Allele Identifier: CA2173753170

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711085G= , CM000677.2:g.44711085G=	GRCh38
NC_000015.9:g.45003283G= , CM000677.1:g.45003283G=	GRCh37
NC_000015.8:g.42790575G=	NCBI36
NG_012920.1:g.4599G=
NG_012920.2:g.4609G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-319C= MANE Select	ENSP00000508024.1:n.-319C=
ENST00000558573.1:n.232C=
XM_011521338.1:c.-319C=	XP_011519640.1:n.-319C=
XM_011521339.1:c.-200C=	XP_011519641.1:n.-200C=
XM_011521340.1:c.-141C=	XP_011519642.1:n.-141C=
XM_011521343.1:c.-403C=	XP_011519645.1:n.-403C=
XM_011521345.1:c.-374C=	XP_011519647.1:n.-374C=
XM_011521338.3:c.-319C=	XP_011519640.1:n.-319C=
XM_011521339.3:c.-200C=	XP_011519641.1:n.-200C=
XM_011521340.3:c.-141C=	XP_011519642.1:n.-141C=
XM_011521343.3:c.-403C=	XP_011519645.1:n.-403C=
XM_011521345.3:c.-374C=	XP_011519647.1:n.-374C=
NM_001387260.1:c.-76+247C=	NP_001374189.1:n.-76+247C=
NM_001387261.1:c.-141C=	NP_001374190.1:n.-141C=
NM_001387262.1:c.-409C=	NP_001374191.1:n.-409C=
NM_001387263.1:c.-319C= MANE Select	NP_001374192.1:n.-319C=