Canonical Allele Identifier: CA399766559

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429151T>A (hg19) ; chr17:g.44351783T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351783T>A , CM000679.2:g.44351783T>A	GRCh38
NC_000017.10:g.42429151T>A , CM000679.1:g.42429151T>A	GRCh37
NC_000017.9:g.39784677T>A	NCBI36
NG_007886.1:g.11661T>A , LRG_661:g.11661T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1167T>A MANE Select	ENSP00000053867.2:p.Cys389Ter
ENST00000639447.1:c.1136+31T>A	ENSP00000492014.1:n.1136+31T>A
ENST00000053867.7:c.1167T>A	ENSP00000053867.2:p.Cys389Ter
ENST00000586443.1:c.608T>A
ENST00000589265.5:c.696T>A	ENSP00000467616.1:p.Cys232Ter
ENST00000589923.1:n.425T>A
NM_002087.3:c.1167T>A	NP_002078.1:p.Cys389Ter
XM_005257253.1:c.1167T>A	XP_005257310.1:p.Cys389Ter
XM_024450730.1:c.1167T>A	XP_024306498.1:p.Cys389Ter
NM_002087.4:c.1167T>A MANE Select	NP_002078.1:p.Cys389Ter