Canonical Allele Identifier: CA2809588885

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352272_44352276del , CM000679.2:g.44352272_44352276del	GRCh38
NC_000017.10:g.42429640_42429644del , CM000679.1:g.42429640_42429644del	GRCh37
NC_000017.9:g.39785166_39785170del	NCBI36
NG_007886.1:g.12150_12154del , LRG_661:g.12150_12154del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1413+24_1413+28del MANE Select	ENSP00000053867.2:n.1413+24_1413+28del
ENST00000639447.1:c.1137-257_1137-253del	ENSP00000492014.1:n.1137-257_1137-253del
ENST00000053867.7:c.1413+24_1413+28del	ENSP00000053867.2:n.1413+24_1413+28del
ENST00000586242.1:c.47+24_47+28del
ENST00000586443.1:c.854+24_854+28del
ENST00000589265.5:c.942+24_942+28del	ENSP00000467616.1:n.942+24_942+28del
NM_002087.3:c.1413+24_1413+28del	NP_002078.1:n.1413+24_1413+28del
XM_005257253.1:c.1413+24_1413+28del	XP_005257310.1:n.1413+24_1413+28del
XM_024450730.1:c.1413+24_1413+28del	XP_024306498.1:n.1413+24_1413+28del
NM_002087.4:c.1413+24_1413+28del MANE Select	NP_002078.1:n.1413+24_1413+28del