Canonical Allele Identifier: CA2173753248

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711335G= , CM000677.2:g.44711335G=	GRCh38
NC_000015.9:g.45003533G= , CM000677.1:g.45003533G=	GRCh37
NC_000015.8:g.42790825G=	NCBI36
NG_012920.1:g.4849G=
NG_012920.2:g.4859G=

Transcript Alleles

HGVS	Amino-acid Change
XM_011521338.1:c.-569C=	XP_011519640.1:n.-569C=
XM_011521339.1:c.-450C=	XP_011519641.1:n.-450C=
XM_011521340.1:c.-391C=	XP_011519642.1:n.-391C=
XM_011521343.1:c.-653C=	XP_011519645.1:n.-653C=
XM_011521345.1:c.-624C=	XP_011519647.1:n.-624C=
XM_011521338.3:c.-569C=	XP_011519640.1:n.-569C=
XM_011521339.3:c.-450C=	XP_011519641.1:n.-450C=
XM_011521340.3:c.-391C=	XP_011519642.1:n.-391C=
XM_011521343.3:c.-653C=	XP_011519645.1:n.-653C=
XM_011521345.3:c.-624C=	XP_011519647.1:n.-624C=
NM_001387260.1:c.-79C=	NP_001374189.1:n.-79C=