Canonical Allele Identifier: CA2042242714
Gene: GNS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.64729111T= , CM000674.2:g.64729111T= GRCh38
NC_000012.11:g.65122891T= , CM000674.1:g.65122891T= GRCh37
NC_000012.10:g.63409158T= NCBI36
NG_008955.1:g.35336A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258145.8:c.1099-54A= MANE Select ENSP00000258145.3:n.1099-54A=
ENST00000258145.7:c.1099-54A= ENSP00000258145.3:n.1099-54A=
ENST00000418919.6:c.931-54A= ENSP00000413130.2:n.931-54A=
ENST00000537823.1:n.44A=
ENST00000540196.5:c.557-5998A=
ENST00000540883.1:n.108A=
ENST00000541781.5:n.1154-54A=
ENST00000542058.5:c.1039-54A= ENSP00000444819.1:n.1039-54A=
ENST00000543646.5:c.1195-54A= ENSP00000438497.1:n.1195-54A=
NM_002076.3:c.1099-54A= NP_002067.1:n.1099-54A=
NM_002076.4:c.1099-54A= MANE Select NP_002067.1:n.1099-54A=
Search 100 bp 5'
Search 100 bp 3'