Canonical Allele Identifier: CA399769447

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429615A>G (hg19) ; chr17:g.44352247A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352247A>G , CM000679.2:g.44352247A>G	GRCh38
NC_000017.10:g.42429615A>G , CM000679.1:g.42429615A>G	GRCh37
NC_000017.9:g.39785141A>G	NCBI36
NG_007886.1:g.12125A>G , LRG_661:g.12125A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1412A>G MANE Select	ENSP00000053867.2:p.His471Arg
ENST00000639447.1:c.1137-282A>G	ENSP00000492014.1:n.1137-282A>G
ENST00000053867.7:c.1412A>G	ENSP00000053867.2:p.His471Arg
ENST00000586242.1:c.46A>G
ENST00000586443.1:c.853A>G
ENST00000589265.5:c.941A>G	ENSP00000467616.1:p.His314Arg
NM_002087.3:c.1412A>G	NP_002078.1:p.His471Arg
XM_005257253.1:c.1412A>G	XP_005257310.1:p.His471Arg
XM_024450730.1:c.1412A>G	XP_024306498.1:p.His471Arg
NM_002087.4:c.1412A>G MANE Select	NP_002078.1:p.His471Arg