Canonical Allele Identifier: CA2638205741

Gene: GRN

Linked Data

• gnomAD v4: 17-44349081-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349081C>A , CM000679.2:g.44349081C>A	GRCh38
NC_000017.10:g.42426449C>A , CM000679.1:g.42426449C>A	GRCh37
NC_000017.9:g.39781975C>A	NCBI36
NG_007886.1:g.8959C>A , LRG_661:g.8959C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.-7-77C>A MANE Select	ENSP00000053867.2:n.-7-77C>A
ENST00000053867.7:c.-7-77C>A	ENSP00000053867.2:n.-7-77C>A
ENST00000585512.5:c.-7-77C>A	ENSP00000467745.1:n.-7-77C>A
ENST00000586782.5:c.-7-77C>A	ENSP00000468318.1:n.-7-77C>A
ENST00000587109.5:c.-7-77C>A	ENSP00000466271.1:n.-7-77C>A
ENST00000587387.5:c.-7-77C>A	ENSP00000467431.1:n.-7-77C>A
ENST00000587518.5:c.-7-77C>A	ENSP00000465518.1:n.-7-77C>A
ENST00000587958.1:n.30-77C>A
ENST00000588143.5:c.-3-81C>A	ENSP00000465375.1:n.-3-81C>A
ENST00000588170.5:n.90-77C>A
ENST00000588237.5:c.-7-77C>A	ENSP00000466611.1:n.-7-77C>A
ENST00000589265.5:c.-7-77C>A	ENSP00000467616.1:n.-7-77C>A
ENST00000589536.5:c.-7-77C>A	ENSP00000466956.1:n.-7-77C>A
ENST00000591740.5:c.-7-77C>A	ENSP00000467022.1:n.-7-77C>A
ENST00000592323.5:n.34-77C>A
ENST00000592783.5:c.-7-77C>A	ENSP00000467870.1:n.-7-77C>A
ENST00000593167.5:c.-7-77C>A	ENSP00000466405.1:n.-7-77C>A
NM_002087.3:c.-7-77C>A	NP_002078.1:n.-7-77C>A
XM_005257253.1:c.-7-77C>A	XP_005257310.1:n.-7-77C>A
XM_024450730.1:c.-7-77C>A	XP_024306498.1:n.-7-77C>A
NM_002087.4:c.-7-77C>A MANE Select	NP_002078.1:n.-7-77C>A