Canonical Allele Identifier: CA399766149

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429107T>A (hg19) ; chr17:g.44351739T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351739T>A , CM000679.2:g.44351739T>A	GRCh38
NC_000017.10:g.42429107T>A , CM000679.1:g.42429107T>A	GRCh37
NC_000017.9:g.39784633T>A	NCBI36
NG_007886.1:g.11617T>A , LRG_661:g.11617T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1123T>A MANE Select	ENSP00000053867.2:p.Ser375Thr
ENST00000639447.1:c.1123T>A	ENSP00000492014.1:p.Ser375Thr
ENST00000053867.7:c.1123T>A	ENSP00000053867.2:p.Ser375Thr
ENST00000586443.1:c.564T>A
ENST00000589265.5:c.652T>A	ENSP00000467616.1:p.Ser218Thr
ENST00000589923.1:n.381T>A
NM_002087.3:c.1123T>A	NP_002078.1:p.Ser375Thr
XM_005257253.1:c.1123T>A	XP_005257310.1:p.Ser375Thr
XM_024450730.1:c.1123T>A	XP_024306498.1:p.Ser375Thr
NM_002087.4:c.1123T>A MANE Select	NP_002078.1:p.Ser375Thr