Canonical Allele Identifier: CA2809588865

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351882_44351883insGTC , CM000679.2:g.44351882_44351883insGTC	GRCh38
NC_000017.10:g.42429250_42429251insGTC , CM000679.1:g.42429250_42429251insGTC	GRCh37
NC_000017.9:g.39784776_39784777insGTC	NCBI36
NG_007886.1:g.11760_11761insGTC , LRG_661:g.11760_11761insGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1179+87_1179+88insGTC MANE Select	ENSP00000053867.2:n.1179+87_1179+88insGTC
ENST00000639447.1:c.1136+130_1136+131insGTC	ENSP00000492014.1:n.1136+130_1136+131insGTC
ENST00000053867.7:c.1179+87_1179+88insGTC	ENSP00000053867.2:n.1179+87_1179+88insGTC
ENST00000586443.1:c.620+87_620+88insGTC
ENST00000589265.5:c.708+87_708+88insGTC	ENSP00000467616.1:n.708+87_708+88insGTC
NM_002087.3:c.1179+87_1179+88insGTC	NP_002078.1:n.1179+87_1179+88insGTC
XM_005257253.1:c.1179+87_1179+88insGTC	XP_005257310.1:n.1179+87_1179+88insGTC
XM_024450730.1:c.1179+87_1179+88insGTC	XP_024306498.1:n.1179+87_1179+88insGTC
NM_002087.4:c.1179+87_1179+88insGTC MANE Select	NP_002078.1:n.1179+87_1179+88insGTC