Canonical Allele Identifier: CA8601997

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351025G>C , CM000679.2:g.44351025G>C	GRCh38
NC_000017.10:g.42428393G>C , CM000679.1:g.42428393G>C	GRCh37
NC_000017.9:g.39783919G>C	NCBI36
NG_007886.1:g.10903G>C , LRG_661:g.10903G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.709-12G>C MANE Select	NP_002078.1:n.709-12G>C
ENST00000053867.8:c.709-12G>C MANE Select	ENSP00000053867.2:n.709-12G>C
NM_002087.3:c.709-12G>C	NP_002078.1:n.709-12G>C
ENST00000053867.7:c.709-12G>C	ENSP00000053867.2:n.709-12G>C
ENST00000585348.1:n.115G>C
ENST00000586443.1:c.150-12G>C
ENST00000586782.5:c.*119-12G>C	ENSP00000468318.1:n.*119-12G>C
ENST00000588237.5:c.511-12G>C	ENSP00000466611.1:n.511-12G>C
ENST00000589265.5:c.463-525G>C	ENSP00000467616.1:n.463-525G>C
ENST00000589923.1:n.30-12G>C
ENST00000590984.1:n.299-12G>C
ENST00000639447.1:c.709-12G>C	ENSP00000492014.1:n.709-12G>C
XM_005257253.1:c.709-12G>C	XP_005257310.1:n.709-12G>C
XM_024450730.1:c.709-12G>C	XP_024306498.1:n.709-12G>C