Canonical Allele Identifier: CA2809588872

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351979_44351980del , CM000679.2:g.44351979_44351980del	GRCh38
NC_000017.10:g.42429347_42429348del , CM000679.1:g.42429347_42429348del	GRCh37
NC_000017.9:g.39784873_39784874del	NCBI36
NG_007886.1:g.11857_11858del , LRG_661:g.11857_11858del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-36_1180-35del MANE Select	ENSP00000053867.2:n.1180-36_1180-35del
ENST00000639447.1:c.1136+227_1136+228del	ENSP00000492014.1:n.1136+227_1136+228del
ENST00000053867.7:c.1180-36_1180-35del	ENSP00000053867.2:n.1180-36_1180-35del
ENST00000586443.1:c.621-36_621-35del
ENST00000589265.5:c.709-36_709-35del	ENSP00000467616.1:n.709-36_709-35del
NM_002087.3:c.1180-36_1180-35del	NP_002078.1:n.1180-36_1180-35del
XM_005257253.1:c.1180-36_1180-35del	XP_005257310.1:n.1180-36_1180-35del
XM_024450730.1:c.1180-36_1180-35del	XP_024306498.1:n.1180-36_1180-35del
NM_002087.4:c.1180-36_1180-35del MANE Select	NP_002078.1:n.1180-36_1180-35del