Canonical Allele Identifier: CA500622309

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429532C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352164C>G , CM000679.2:g.44352164C>G	GRCh38
NC_000017.10:g.42429532C>G , CM000679.1:g.42429532C>G	GRCh37
NC_000017.9:g.39785058C>G	NCBI36
NG_007886.1:g.12042C>G , LRG_661:g.12042C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1329C>G MANE Select	ENSP00000053867.2:p.Gly443=
ENST00000639447.1:c.1137-365C>G	ENSP00000492014.1:n.1137-365C>G
ENST00000053867.7:c.1329C>G	ENSP00000053867.2:p.Gly443=
ENST00000586443.1:c.770C>G
ENST00000589265.5:c.858C>G	ENSP00000467616.1:p.Gly286=
NM_002087.3:c.1329C>G	NP_002078.1:p.Gly443=
XM_005257253.1:c.1329C>G	XP_005257310.1:p.Gly443=
XM_024450730.1:c.1329C>G	XP_024306498.1:p.Gly443=
NM_002087.4:c.1329C>G MANE Select	NP_002078.1:p.Gly443=