Canonical Allele Identifier: CA2173753218

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711260G= , CM000677.2:g.44711260G=	GRCh38
NC_000015.9:g.45003458G= , CM000677.1:g.45003458G=	GRCh37
NC_000015.8:g.42790750G=	NCBI36
NG_012920.1:g.4774G=
NG_012920.2:g.4784G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-494C= MANE Select	ENSP00000508024.1:n.-494C=
ENST00000558573.1:n.57C=
XM_011521338.1:c.-494C=	XP_011519640.1:n.-494C=
XM_011521339.1:c.-375C=	XP_011519641.1:n.-375C=
XM_011521340.1:c.-316C=	XP_011519642.1:n.-316C=
XM_011521343.1:c.-578C=	XP_011519645.1:n.-578C=
XM_011521345.1:c.-549C=	XP_011519647.1:n.-549C=
XM_011521338.3:c.-494C=	XP_011519640.1:n.-494C=
XM_011521339.3:c.-375C=	XP_011519641.1:n.-375C=
XM_011521340.3:c.-316C=	XP_011519642.1:n.-316C=
XM_011521343.3:c.-578C=	XP_011519645.1:n.-578C=
XM_011521345.3:c.-549C=	XP_011519647.1:n.-549C=
NM_001387260.1:c.-76+72C=	NP_001374189.1:n.-76+72C=
NM_001387261.1:c.-316C=	NP_001374190.1:n.-316C=
NM_001387262.1:c.-584C=	NP_001374191.1:n.-584C=
NM_001387263.1:c.-494C= MANE Select	NP_001374192.1:n.-494C=