Canonical Allele Identifier: CA2638210098

Gene: GRN

Linked Data

• gnomAD v4: 17-44351954-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351954G>T , CM000679.2:g.44351954G>T	GRCh38
NC_000017.10:g.42429322G>T , CM000679.1:g.42429322G>T	GRCh37
NC_000017.9:g.39784848G>T	NCBI36
NG_007886.1:g.11832G>T , LRG_661:g.11832G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-61G>T MANE Select	ENSP00000053867.2:n.1180-61G>T
ENST00000639447.1:c.1136+202G>T	ENSP00000492014.1:n.1136+202G>T
ENST00000053867.7:c.1180-61G>T	ENSP00000053867.2:n.1180-61G>T
ENST00000586443.1:c.621-61G>T
ENST00000589265.5:c.709-61G>T	ENSP00000467616.1:n.709-61G>T
NM_002087.3:c.1180-61G>T	NP_002078.1:n.1180-61G>T
XM_005257253.1:c.1180-61G>T	XP_005257310.1:n.1180-61G>T
XM_024450730.1:c.1180-61G>T	XP_024306498.1:n.1180-61G>T
NM_002087.4:c.1180-61G>T MANE Select	NP_002078.1:n.1180-61G>T