Canonical Allele Identifier: CA399765397

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429018T>A (hg19) ; chr17:g.44351650T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351650T>A , CM000679.2:g.44351650T>A	GRCh38
NC_000017.10:g.42429018T>A , CM000679.1:g.42429018T>A	GRCh37
NC_000017.9:g.39784544T>A	NCBI36
NG_007886.1:g.11528T>A , LRG_661:g.11528T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1034T>A MANE Select	ENSP00000053867.2:p.Met345Lys
ENST00000639447.1:c.1034T>A	ENSP00000492014.1:p.Met345Lys
ENST00000053867.7:c.1034T>A	ENSP00000053867.2:p.Met345Lys
ENST00000586443.1:c.475T>A
ENST00000589265.5:c.563T>A	ENSP00000467616.1:p.Met188Lys
ENST00000589923.1:n.292T>A
NM_002087.3:c.1034T>A	NP_002078.1:p.Met345Lys
XM_005257253.1:c.1034T>A	XP_005257310.1:p.Met345Lys
XM_024450730.1:c.1034T>A	XP_024306498.1:p.Met345Lys
NM_002087.4:c.1034T>A MANE Select	NP_002078.1:p.Met345Lys