Canonical Allele Identifier: CA2261354401

Gene: GRN

Linked Data

• dbSNP Id: rs2048379059

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351927_44351929dup , CM000679.2:g.44351927_44351929dup	GRCh38
NC_000017.10:g.42429295_42429297dup , CM000679.1:g.42429295_42429297dup	GRCh37
NC_000017.9:g.39784821_39784823dup	NCBI36
NG_007886.1:g.11805_11807dup , LRG_661:g.11805_11807dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-88_1180-86dup MANE Select	ENSP00000053867.2:n.1180-88_1180-86dup
ENST00000639447.1:c.1136+175_1136+177dup	ENSP00000492014.1:n.1136+175_1136+177dup
ENST00000053867.7:c.1180-88_1180-86dup	ENSP00000053867.2:n.1180-88_1180-86dup
ENST00000586443.1:c.621-88_621-86dup
ENST00000589265.5:c.709-88_709-86dup	ENSP00000467616.1:n.709-88_709-86dup
NM_002087.3:c.1180-88_1180-86dup	NP_002078.1:n.1180-88_1180-86dup
XM_005257253.1:c.1180-88_1180-86dup	XP_005257310.1:n.1180-88_1180-86dup
XM_024450730.1:c.1180-88_1180-86dup	XP_024306498.1:n.1180-88_1180-86dup
NM_002087.4:c.1180-88_1180-86dup MANE Select	NP_002078.1:n.1180-88_1180-86dup