Canonical Allele Identifier: CA2638205729

Gene: GRN

Linked Data

• gnomAD v4: 17-44349070-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349070T>C , CM000679.2:g.44349070T>C	GRCh38
NC_000017.10:g.42426438T>C , CM000679.1:g.42426438T>C	GRCh37
NC_000017.9:g.39781964T>C	NCBI36
NG_007886.1:g.8948T>C , LRG_661:g.8948T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.-7-88T>C MANE Select	ENSP00000053867.2:n.-7-88T>C
ENST00000053867.7:c.-7-88T>C	ENSP00000053867.2:n.-7-88T>C
ENST00000585512.5:c.-7-88T>C	ENSP00000467745.1:n.-7-88T>C
ENST00000586782.5:c.-7-88T>C	ENSP00000468318.1:n.-7-88T>C
ENST00000587109.5:c.-7-88T>C	ENSP00000466271.1:n.-7-88T>C
ENST00000587387.5:c.-7-88T>C	ENSP00000467431.1:n.-7-88T>C
ENST00000587518.5:c.-7-88T>C	ENSP00000465518.1:n.-7-88T>C
ENST00000587958.1:n.30-88T>C
ENST00000588143.5:c.-3-92T>C	ENSP00000465375.1:n.-3-92T>C
ENST00000588170.5:n.90-88T>C
ENST00000588237.5:c.-7-88T>C	ENSP00000466611.1:n.-7-88T>C
ENST00000589265.5:c.-7-88T>C	ENSP00000467616.1:n.-7-88T>C
ENST00000589536.5:c.-7-88T>C	ENSP00000466956.1:n.-7-88T>C
ENST00000591740.5:c.-7-88T>C	ENSP00000467022.1:n.-7-88T>C
ENST00000592323.5:n.34-88T>C
ENST00000592783.5:c.-7-88T>C	ENSP00000467870.1:n.-7-88T>C
ENST00000593167.5:c.-7-88T>C	ENSP00000466405.1:n.-7-88T>C
NM_002087.3:c.-7-88T>C	NP_002078.1:n.-7-88T>C
XM_005257253.1:c.-7-88T>C	XP_005257310.1:n.-7-88T>C
XM_024450730.1:c.-7-88T>C	XP_024306498.1:n.-7-88T>C
NM_002087.4:c.-7-88T>C MANE Select	NP_002078.1:n.-7-88T>C