Canonical Allele Identifier: CA2173753194

Gene: PATL2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711170G= , CM000677.2:g.44711170G=	GRCh38
NC_000015.9:g.45003368G= , CM000677.1:g.45003368G=	GRCh37
NC_000015.8:g.42790660G=	NCBI36
NG_012920.1:g.4684G=
NG_012920.2:g.4694G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-404C= MANE Select	ENSP00000508024.1:n.-404C=
ENST00000558573.1:n.147C=
XM_011521338.1:c.-404C=	XP_011519640.1:n.-404C=
XM_011521339.1:c.-285C=	XP_011519641.1:n.-285C=
XM_011521340.1:c.-226C=	XP_011519642.1:n.-226C=
XM_011521343.1:c.-488C=	XP_011519645.1:n.-488C=
XM_011521345.1:c.-459C=	XP_011519647.1:n.-459C=
XM_011521338.3:c.-404C=	XP_011519640.1:n.-404C=
XM_011521339.3:c.-285C=	XP_011519641.1:n.-285C=
XM_011521340.3:c.-226C=	XP_011519642.1:n.-226C=
XM_011521343.3:c.-488C=	XP_011519645.1:n.-488C=
XM_011521345.3:c.-459C=	XP_011519647.1:n.-459C=
NM_001387260.1:c.-76+162C=	NP_001374189.1:n.-76+162C=
NM_001387261.1:c.-226C=	NP_001374190.1:n.-226C=
NM_001387262.1:c.-494C=	NP_001374191.1:n.-494C=
NM_001387263.1:c.-404C= MANE Select	NP_001374192.1:n.-404C=