Canonical Allele Identifier: CA399766609

Gene: GRN

Linked Data

• COSMIC: COSM706162
• MyVariant Identifiers: chr17:g.42429158C>A (hg19) ; chr17:g.44351790C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351790C>A , CM000679.2:g.44351790C>A	GRCh38
NC_000017.10:g.42429158C>A , CM000679.1:g.42429158C>A	GRCh37
NC_000017.9:g.39784684C>A	NCBI36
NG_007886.1:g.11668C>A , LRG_661:g.11668C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1174C>A MANE Select	ENSP00000053867.2:p.Pro392Thr
ENST00000639447.1:c.1136+38C>A	ENSP00000492014.1:n.1136+38C>A
ENST00000053867.7:c.1174C>A	ENSP00000053867.2:p.Pro392Thr
ENST00000586443.1:c.615C>A
ENST00000589265.5:c.703C>A	ENSP00000467616.1:p.Pro235Thr
ENST00000589923.1:n.432C>A
NM_002087.3:c.1174C>A	NP_002078.1:p.Pro392Thr
XM_005257253.1:c.1174C>A	XP_005257310.1:p.Pro392Thr
XM_024450730.1:c.1174C>A	XP_024306498.1:p.Pro392Thr
NM_002087.4:c.1174C>A MANE Select	NP_002078.1:p.Pro392Thr