Canonical Allele Identifier: CA399764114

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42428071G>C (hg19) ; chr17:g.44350703G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350703G>C , CM000679.2:g.44350703G>C	GRCh38
NC_000017.10:g.42428071G>C , CM000679.1:g.42428071G>C	GRCh37
NC_000017.9:g.39783597G>C	NCBI36
NG_007886.1:g.10581G>C , LRG_661:g.10581G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.611G>C MANE Select	ENSP00000053867.2:p.Ser204Thr
ENST00000639447.1:c.611G>C	ENSP00000492014.1:p.Ser204Thr
ENST00000053867.7:c.611G>C	ENSP00000053867.2:p.Ser204Thr
ENST00000586443.1:c.52G>C
ENST00000586782.5:c.*21G>C	ENSP00000468318.1:n.*21G>C
ENST00000588237.5:c.413G>C	ENSP00000466611.1:p.Ser138Thr
ENST00000589265.5:c.462+363G>C	ENSP00000467616.1:n.462+363G>C
ENST00000590984.1:n.201G>C
NM_002087.3:c.611G>C	NP_002078.1:p.Ser204Thr
XM_005257253.1:c.611G>C	XP_005257310.1:p.Ser204Thr
XM_024450730.1:c.611G>C	XP_024306498.1:p.Ser204Thr
NM_002087.4:c.611G>C MANE Select	NP_002078.1:p.Ser204Thr