Canonical Allele Identifier: CA2839170885

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351033T>C , CM000679.2:g.44351033T>C	GRCh38
NC_000017.10:g.42428401T>C , CM000679.1:g.42428401T>C	GRCh37
NC_000017.9:g.39783927T>C	NCBI36
NG_007886.1:g.10911T>C , LRG_661:g.10911T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.709-4T>C MANE Select	ENSP00000053867.2:n.709-4T>C
ENST00000639447.1:c.709-4T>C	ENSP00000492014.1:n.709-4T>C
ENST00000053867.7:c.709-4T>C	ENSP00000053867.2:n.709-4T>C
ENST00000585348.1:n.123T>C
ENST00000586443.1:c.150-4T>C
ENST00000586782.5:c.*119-4T>C	ENSP00000468318.1:n.*119-4T>C
ENST00000588237.5:c.511-4T>C	ENSP00000466611.1:n.511-4T>C
ENST00000589265.5:c.463-517T>C	ENSP00000467616.1:n.463-517T>C
ENST00000589923.1:n.30-4T>C
ENST00000590984.1:n.299-4T>C
NM_002087.3:c.709-4T>C	NP_002078.1:n.709-4T>C
XM_005257253.1:c.709-4T>C	XP_005257310.1:n.709-4T>C
XM_024450730.1:c.709-4T>C	XP_024306498.1:n.709-4T>C
NM_002087.4:c.709-4T>C MANE Select	NP_002078.1:n.709-4T>C