Canonical Allele Identifier: CA2576290532

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351858_44351859del , CM000679.2:g.44351858_44351859del	GRCh38
NC_000017.10:g.42429226_42429227del , CM000679.1:g.42429226_42429227del	GRCh37
NC_000017.9:g.39784752_39784753del	NCBI36
NG_007886.1:g.11736_11737del , LRG_661:g.11736_11737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+63_1179+64del MANE Select	ENSP00000053867.2:n.1179+63_1179+64del
ENST00000639447.1:c.1136+106_1136+107del	ENSP00000492014.1:n.1136+106_1136+107del
ENST00000053867.7:c.1179+63_1179+64del	ENSP00000053867.2:n.1179+63_1179+64del
ENST00000586443.1:c.620+63_620+64del
ENST00000589265.5:c.708+63_708+64del	ENSP00000467616.1:n.708+63_708+64del
NM_002087.3:c.1179+63_1179+64del	NP_002078.1:n.1179+63_1179+64del
XM_005257253.1:c.1179+63_1179+64del	XP_005257310.1:n.1179+63_1179+64del
XM_024450730.1:c.1179+63_1179+64del	XP_024306498.1:n.1179+63_1179+64del
NM_002087.4:c.1179+63_1179+64del MANE Select	NP_002078.1:n.1179+63_1179+64del