Canonical Allele Identifier: CA2173753200

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711185C= , CM000677.2:g.44711185C=	GRCh38
NC_000015.9:g.45003383C= , CM000677.1:g.45003383C=	GRCh37
NC_000015.8:g.42790675C=	NCBI36
NG_012920.1:g.4699C=
NG_012920.2:g.4709C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-419G= MANE Select	ENSP00000508024.1:n.-419G=
ENST00000558573.1:n.132G=
XM_011521338.1:c.-419G=	XP_011519640.1:n.-419G=
XM_011521339.1:c.-300G=	XP_011519641.1:n.-300G=
XM_011521340.1:c.-241G=	XP_011519642.1:n.-241G=
XM_011521343.1:c.-503G=	XP_011519645.1:n.-503G=
XM_011521345.1:c.-474G=	XP_011519647.1:n.-474G=
XM_011521338.3:c.-419G=	XP_011519640.1:n.-419G=
XM_011521339.3:c.-300G=	XP_011519641.1:n.-300G=
XM_011521340.3:c.-241G=	XP_011519642.1:n.-241G=
XM_011521343.3:c.-503G=	XP_011519645.1:n.-503G=
XM_011521345.3:c.-474G=	XP_011519647.1:n.-474G=
NM_001387260.1:c.-76+147G=	NP_001374189.1:n.-76+147G=
NM_001387261.1:c.-241G=	NP_001374190.1:n.-241G=
NM_001387262.1:c.-509G=	NP_001374191.1:n.-509G=
NM_001387263.1:c.-419G= MANE Select	NP_001374192.1:n.-419G=