Canonical Allele Identifier: CA2173753227

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711293C= , CM000677.2:g.44711293C=	GRCh38
NC_000015.9:g.45003491C= , CM000677.1:g.45003491C=	GRCh37
NC_000015.8:g.42790783C=	NCBI36
NG_012920.1:g.4807C=
NG_012920.2:g.4817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-527G= MANE Select	ENSP00000508024.1:n.-527G=
ENST00000558573.1:n.24G=
XM_011521338.1:c.-527G=	XP_011519640.1:n.-527G=
XM_011521339.1:c.-408G=	XP_011519641.1:n.-408G=
XM_011521340.1:c.-349G=	XP_011519642.1:n.-349G=
XM_011521343.1:c.-611G=	XP_011519645.1:n.-611G=
XM_011521345.1:c.-582G=	XP_011519647.1:n.-582G=
XM_011521338.3:c.-527G=	XP_011519640.1:n.-527G=
XM_011521339.3:c.-408G=	XP_011519641.1:n.-408G=
XM_011521340.3:c.-349G=	XP_011519642.1:n.-349G=
XM_011521343.3:c.-611G=	XP_011519645.1:n.-611G=
XM_011521345.3:c.-582G=	XP_011519647.1:n.-582G=
NM_001387260.1:c.-76+39G=	NP_001374189.1:n.-76+39G=
NM_001387261.1:c.-349G=	NP_001374190.1:n.-349G=
NM_001387262.1:c.-617G=	NP_001374191.1:n.-617G=
NM_001387263.1:c.-527G= MANE Select	NP_001374192.1:n.-527G=