Canonical Allele Identifier: CA2809588881

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352140_44352141del , CM000679.2:g.44352140_44352141del	GRCh38
NC_000017.10:g.42429508_42429509del , CM000679.1:g.42429508_42429509del	GRCh37
NC_000017.9:g.39785034_39785035del	NCBI36
NG_007886.1:g.12018_12019del , LRG_661:g.12018_12019del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1305_1306del MANE Select	ENSP00000053867.2:p.Leu436IlefsTer9
ENST00000639447.1:c.1137-389_1137-388del	ENSP00000492014.1:n.1137-389_1137-388del
ENST00000053867.7:c.1305_1306del	ENSP00000053867.2:p.Leu436IlefsTer9
ENST00000586443.1:c.746_747del
ENST00000589265.5:c.834_835del	ENSP00000467616.1:p.Leu279IlefsTer9
NM_002087.3:c.1305_1306del	NP_002078.1:p.Leu436IlefsTer9
XM_005257253.1:c.1305_1306del	XP_005257310.1:p.Leu436IlefsTer9
XM_024450730.1:c.1305_1306del	XP_024306498.1:p.Leu436IlefsTer9
NM_002087.4:c.1305_1306del MANE Select	NP_002078.1:p.Leu436IlefsTer9