Canonical Allele Identifier: CA2146887209

Gene: LIN52

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74085267G= , CM000676.2:g.74085267G=	GRCh38
NC_000014.8:g.74551970G= , CM000676.1:g.74551970G=	GRCh37
NC_000014.7:g.73621723G=	NCBI36
NG_012257.2:g.4227C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555028.7:c.19+274G= MANE Select	ENSP00000451812.2:n.19+274G=
ENST00000554938.2:c.19+274G=	ENSP00000452513.2:n.19+274G=
ENST00000555028.6:c.19+274G=	ENSP00000451812.2:n.19+274G=
ENST00000674221.1:c.31+274G=	ENSP00000501511.1:n.31+274G=
ENST00000553404.5:n.308G=
ENST00000554076.5:n.31+274G=
ENST00000554938.1:c.38+274G=
ENST00000555028.5:c.31+274G=	ENSP00000451812.1:n.31+274G=
NM_001024674.2:c.31+274G=	NP_001019845.1:n.31+274G=
XM_011537320.1:c.127+274G=	XP_011535622.1:n.127+274G=
XM_011537321.1:c.127+274G=	XP_011535623.1:n.127+274G=
XM_011537322.1:c.127+274G=	XP_011535624.1:n.127+274G=
XM_011537320.3:c.127+274G=	XP_011535622.1:n.127+274G=
XM_011537321.3:c.127+274G=	XP_011535623.1:n.127+274G=
XM_011537322.2:c.31+274G=	XP_011535624.2:n.31+274G=
XM_017021763.2:c.31+274G=	XP_016877252.1:n.31+274G=
XM_017021764.1:c.31+274G=	XP_016877253.1:n.31+274G=
NM_001024674.3:c.19+274G= MANE Select	NP_001019845.2:n.19+274G=
NM_001372005.1:c.19+274G=	NP_001358934.1:n.19+274G=
NM_001372006.1:c.19+274G=	NP_001358935.1:n.19+274G=