Canonical Allele Identifier: CA2173753193

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711169G= , CM000677.2:g.44711169G=	GRCh38
NC_000015.9:g.45003367G= , CM000677.1:g.45003367G=	GRCh37
NC_000015.8:g.42790659G=	NCBI36
NG_012920.1:g.4683G=
NG_012920.2:g.4693G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-403C= MANE Select	ENSP00000508024.1:n.-403C=
ENST00000558573.1:n.148C=
XM_011521338.1:c.-403C=	XP_011519640.1:n.-403C=
XM_011521339.1:c.-284C=	XP_011519641.1:n.-284C=
XM_011521340.1:c.-225C=	XP_011519642.1:n.-225C=
XM_011521343.1:c.-487C=	XP_011519645.1:n.-487C=
XM_011521345.1:c.-458C=	XP_011519647.1:n.-458C=
XM_011521338.3:c.-403C=	XP_011519640.1:n.-403C=
XM_011521339.3:c.-284C=	XP_011519641.1:n.-284C=
XM_011521340.3:c.-225C=	XP_011519642.1:n.-225C=
XM_011521343.3:c.-487C=	XP_011519645.1:n.-487C=
XM_011521345.3:c.-458C=	XP_011519647.1:n.-458C=
NM_001387260.1:c.-76+163C=	NP_001374189.1:n.-76+163C=
NM_001387261.1:c.-225C=	NP_001374190.1:n.-225C=
NM_001387262.1:c.-493C=	NP_001374191.1:n.-493C=
NM_001387263.1:c.-403C= MANE Select	NP_001374192.1:n.-403C=