Canonical Allele Identifier: CA983969694

Gene: GRN

Linked Data

• dbSNP Id: rs2048346480
• gnomAD v3: 17-44349082-T-G
• gnomAD v4: 17-44349082-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349082T>G , CM000679.2:g.44349082T>G	GRCh38
NC_000017.10:g.42426450T>G , CM000679.1:g.42426450T>G	GRCh37
NC_000017.9:g.39781976T>G	NCBI36
NG_007886.1:g.8960T>G , LRG_661:g.8960T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.-7-76T>G MANE Select	ENSP00000053867.2:n.-7-76T>G
ENST00000053867.7:c.-7-76T>G	ENSP00000053867.2:n.-7-76T>G
ENST00000585512.5:c.-7-76T>G	ENSP00000467745.1:n.-7-76T>G
ENST00000586782.5:c.-7-76T>G	ENSP00000468318.1:n.-7-76T>G
ENST00000587109.5:c.-7-76T>G	ENSP00000466271.1:n.-7-76T>G
ENST00000587387.5:c.-7-76T>G	ENSP00000467431.1:n.-7-76T>G
ENST00000587518.5:c.-7-76T>G	ENSP00000465518.1:n.-7-76T>G
ENST00000587958.1:n.30-76T>G
ENST00000588143.5:c.-3-80T>G	ENSP00000465375.1:n.-3-80T>G
ENST00000588170.5:n.90-76T>G
ENST00000588237.5:c.-7-76T>G	ENSP00000466611.1:n.-7-76T>G
ENST00000589265.5:c.-7-76T>G	ENSP00000467616.1:n.-7-76T>G
ENST00000589536.5:c.-7-76T>G	ENSP00000466956.1:n.-7-76T>G
ENST00000591740.5:c.-7-76T>G	ENSP00000467022.1:n.-7-76T>G
ENST00000592323.5:n.34-76T>G
ENST00000592783.5:c.-7-76T>G	ENSP00000467870.1:n.-7-76T>G
ENST00000593167.5:c.-7-76T>G	ENSP00000466405.1:n.-7-76T>G
NM_002087.3:c.-7-76T>G	NP_002078.1:n.-7-76T>G
XM_005257253.1:c.-7-76T>G	XP_005257310.1:n.-7-76T>G
XM_024450730.1:c.-7-76T>G	XP_024306498.1:n.-7-76T>G
NM_002087.4:c.-7-76T>G MANE Select	NP_002078.1:n.-7-76T>G