Canonical Allele Identifier: CA399765824

Gene: GRN

Linked Data

• dbSNP Id: rs2048376294
• MyVariant Identifiers: chr17:g.42429070A>C (hg19) ; chr17:g.44351702A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351702A>C , CM000679.2:g.44351702A>C	GRCh38
NC_000017.10:g.42429070A>C , CM000679.1:g.42429070A>C	GRCh37
NC_000017.9:g.39784596A>C	NCBI36
NG_007886.1:g.11580A>C , LRG_661:g.11580A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1086A>C MANE Select	ENSP00000053867.2:p.Arg362Ser
ENST00000639447.1:c.1086A>C	ENSP00000492014.1:p.Arg362Ser
ENST00000053867.7:c.1086A>C	ENSP00000053867.2:p.Arg362Ser
ENST00000586443.1:c.527A>C
ENST00000589265.5:c.615A>C	ENSP00000467616.1:p.Arg205Ser
ENST00000589923.1:n.344A>C
NM_002087.3:c.1086A>C	NP_002078.1:p.Arg362Ser
XM_005257253.1:c.1086A>C	XP_005257310.1:p.Arg362Ser
XM_024450730.1:c.1086A>C	XP_024306498.1:p.Arg362Ser
NM_002087.4:c.1086A>C MANE Select	NP_002078.1:p.Arg362Ser