Canonical Allele Identifier: CA2638210100

Gene: GRN

Linked Data

• gnomAD v4: 17-44351956-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351956C>A , CM000679.2:g.44351956C>A	GRCh38
NC_000017.10:g.42429324C>A , CM000679.1:g.42429324C>A	GRCh37
NC_000017.9:g.39784850C>A	NCBI36
NG_007886.1:g.11834C>A , LRG_661:g.11834C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1180-59C>A MANE Select	ENSP00000053867.2:n.1180-59C>A
ENST00000639447.1:c.1136+204C>A	ENSP00000492014.1:n.1136+204C>A
ENST00000053867.7:c.1180-59C>A	ENSP00000053867.2:n.1180-59C>A
ENST00000586443.1:c.621-59C>A
ENST00000589265.5:c.709-59C>A	ENSP00000467616.1:n.709-59C>A
NM_002087.3:c.1180-59C>A	NP_002078.1:n.1180-59C>A
XM_005257253.1:c.1180-59C>A	XP_005257310.1:n.1180-59C>A
XM_024450730.1:c.1180-59C>A	XP_024306498.1:n.1180-59C>A
NM_002087.4:c.1180-59C>A MANE Select	NP_002078.1:n.1180-59C>A