Canonical Allele Identifier: CA385604276

Gene: GNS

Linked Data

• gnomAD v4: 12-64728999-A-T
• MyVariant Identifiers: chr12:g.65122779A>T (hg19) ; chr12:g.64728999A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64728999A>T , CM000674.2:g.64728999A>T	GRCh38
NC_000012.11:g.65122779A>T , CM000674.1:g.65122779A>T	GRCh37
NC_000012.10:g.63409046A>T	NCBI36
NG_008955.1:g.35448T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258145.8:c.1157T>A MANE Select	ENSP00000258145.3:p.Leu386Gln
ENST00000258145.7:c.1157T>A	ENSP00000258145.3:p.Leu386Gln
ENST00000418919.6:c.989T>A	ENSP00000413130.2:p.Leu330Gln
ENST00000537823.1:n.156T>A
ENST00000540196.5:c.557-5886T>A
ENST00000540883.1:n.220T>A
ENST00000541781.5:n.1212T>A
ENST00000542058.5:c.1097T>A	ENSP00000444819.1:p.Leu366Gln
ENST00000543646.5:c.1253T>A	ENSP00000438497.1:p.Leu418Gln
NM_002076.3:c.1157T>A	NP_002067.1:p.Leu386Gln
NM_002076.4:c.1157T>A MANE Select	NP_002067.1:p.Leu386Gln