Canonical Allele Identifier: CA399766041

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429095A>C (hg19) ; chr17:g.44351727A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351727A>C , CM000679.2:g.44351727A>C	GRCh38
NC_000017.10:g.42429095A>C , CM000679.1:g.42429095A>C	GRCh37
NC_000017.9:g.39784621A>C	NCBI36
NG_007886.1:g.11605A>C , LRG_661:g.11605A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1111A>C MANE Select	ENSP00000053867.2:p.Ser371Arg
ENST00000639447.1:c.1111A>C	ENSP00000492014.1:p.Ser371Arg
ENST00000053867.7:c.1111A>C	ENSP00000053867.2:p.Ser371Arg
ENST00000586443.1:c.552A>C
ENST00000589265.5:c.640A>C	ENSP00000467616.1:p.Ser214Arg
ENST00000589923.1:n.369A>C
NM_002087.3:c.1111A>C	NP_002078.1:p.Ser371Arg
XM_005257253.1:c.1111A>C	XP_005257310.1:p.Ser371Arg
XM_024450730.1:c.1111A>C	XP_024306498.1:p.Ser371Arg
NM_002087.4:c.1111A>C MANE Select	NP_002078.1:p.Ser371Arg