Canonical Allele Identifier: CA399764551

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42428416C>A (hg19) ; chr17:g.44351048C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351048C>A , CM000679.2:g.44351048C>A	GRCh38
NC_000017.10:g.42428416C>A , CM000679.1:g.42428416C>A	GRCh37
NC_000017.9:g.39783942C>A	NCBI36
NG_007886.1:g.10926C>A , LRG_661:g.10926C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.720C>A MANE Select	ENSP00000053867.2:p.Cys240Ter
ENST00000639447.1:c.720C>A	ENSP00000492014.1:p.Cys240Ter
ENST00000053867.7:c.720C>A	ENSP00000053867.2:p.Cys240Ter
ENST00000585348.1:n.138C>A
ENST00000586443.1:c.161C>A
ENST00000586782.5:c.*130C>A	ENSP00000468318.1:n.*130C>A
ENST00000589265.5:c.463-502C>A	ENSP00000467616.1:n.463-502C>A
ENST00000589923.1:n.41C>A
ENST00000590984.1:n.310C>A
NM_002087.3:c.720C>A	NP_002078.1:p.Cys240Ter
XM_005257253.1:c.720C>A	XP_005257310.1:p.Cys240Ter
XM_024450730.1:c.720C>A	XP_024306498.1:p.Cys240Ter
NM_002087.4:c.720C>A MANE Select	NP_002078.1:p.Cys240Ter