Canonical Allele Identifier: CA399769266

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429575C>G (hg19) ; chr17:g.44352207C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352207C>G , CM000679.2:g.44352207C>G	GRCh38
NC_000017.10:g.42429575C>G , CM000679.1:g.42429575C>G	GRCh37
NC_000017.9:g.39785101C>G	NCBI36
NG_007886.1:g.12085C>G , LRG_661:g.12085C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1372C>G MANE Select	ENSP00000053867.2:p.Pro458Ala
ENST00000639447.1:c.1137-322C>G	ENSP00000492014.1:n.1137-322C>G
ENST00000053867.7:c.1372C>G	ENSP00000053867.2:p.Pro458Ala
ENST00000586242.1:c.6C>G
ENST00000586443.1:c.813C>G
ENST00000589265.5:c.901C>G	ENSP00000467616.1:p.Pro301Ala
NM_002087.3:c.1372C>G	NP_002078.1:p.Pro458Ala
XM_005257253.1:c.1372C>G	XP_005257310.1:p.Pro458Ala
XM_024450730.1:c.1372C>G	XP_024306498.1:p.Pro458Ala
NM_002087.4:c.1372C>G MANE Select	NP_002078.1:p.Pro458Ala