Canonical Allele Identifier: CA2261354298

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351730_44351731delinsTG , CM000679.2:g.44351730_44351731delinsTG	GRCh38
NC_000017.10:g.42429098_42429099delinsTG , CM000679.1:g.42429098_42429099delinsTG	GRCh37
NC_000017.9:g.39784624_39784625delinsTG	NCBI36
NG_007886.1:g.11608_11609delinsTG , LRG_661:g.11608_11609delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1114_1115delinsTG MANE Select	ENSP00000053867.2:p.Cys372=
ENST00000639447.1:c.1114_1115delinsTG	ENSP00000492014.1:p.Cys372=
ENST00000053867.7:c.1114_1115delinsTG	ENSP00000053867.2:p.Cys372=
ENST00000586443.1:c.555_556delinsTG
ENST00000589265.5:c.643_644delinsTG	ENSP00000467616.1:p.Cys215=
ENST00000589923.1:n.372_373delinsTG
NM_002087.3:c.1114_1115delinsTG	NP_002078.1:p.Cys372=
XM_005257253.1:c.1114_1115delinsTG	XP_005257310.1:p.Cys372=
XM_024450730.1:c.1114_1115delinsTG	XP_024306498.1:p.Cys372=
NM_002087.4:c.1114_1115delinsTG MANE Select	NP_002078.1:p.Cys372=