Canonical Allele Identifier: CA2261354540

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352190_44352191delinsTG , CM000679.2:g.44352190_44352191delinsTG	GRCh38
NC_000017.10:g.42429558_42429559delinsTG , CM000679.1:g.42429558_42429559delinsTG	GRCh37
NC_000017.9:g.39785084_39785085delinsTG	NCBI36
NG_007886.1:g.12068_12069delinsTG , LRG_661:g.12068_12069delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1355_1356delinsTG MANE Select	ENSP00000053867.2:p.Val452=
ENST00000639447.1:c.1137-339_1137-338delinsTG	ENSP00000492014.1:n.1137-339_1137-338delinsTG
ENST00000053867.7:c.1355_1356delinsTG	ENSP00000053867.2:p.Val452=
ENST00000586443.1:c.796_797delinsTG
ENST00000589265.5:c.884_885delinsTG	ENSP00000467616.1:p.Val295=
NM_002087.3:c.1355_1356delinsTG	NP_002078.1:p.Val452=
XM_005257253.1:c.1355_1356delinsTG	XP_005257310.1:p.Val452=
XM_024450730.1:c.1355_1356delinsTG	XP_024306498.1:p.Val452=
NM_002087.4:c.1355_1356delinsTG MANE Select	NP_002078.1:p.Val452=