Canonical Allele Identifier: CA2042242702

Gene: GNS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64729096_64729097delinsGT , CM000674.2:g.64729096_64729097delinsGT	GRCh38
NC_000012.11:g.65122876_65122877delinsGT , CM000674.1:g.65122876_65122877delinsGT	GRCh37
NC_000012.10:g.63409143_63409144delinsGT	NCBI36
NG_008955.1:g.35350_35351delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258145.8:c.1099-40_1099-39delinsAC MANE Select	ENSP00000258145.3:n.1099-40_1099-39delinsAC
ENST00000258145.7:c.1099-40_1099-39delinsAC	ENSP00000258145.3:n.1099-40_1099-39delinsAC
ENST00000418919.6:c.931-40_931-39delinsAC	ENSP00000413130.2:n.931-40_931-39delinsAC
ENST00000537823.1:n.58_59delinsAC
ENST00000540196.5:c.557-5984_557-5983delinsAC
ENST00000540883.1:n.122_123delinsAC
ENST00000541781.5:n.1154-40_1154-39delinsAC
ENST00000542058.5:c.1039-40_1039-39delinsAC	ENSP00000444819.1:n.1039-40_1039-39delinsAC
ENST00000543646.5:c.1195-40_1195-39delinsAC	ENSP00000438497.1:n.1195-40_1195-39delinsAC
NM_002076.3:c.1099-40_1099-39delinsAC	NP_002067.1:n.1099-40_1099-39delinsAC
NM_002076.4:c.1099-40_1099-39delinsAC MANE Select	NP_002067.1:n.1099-40_1099-39delinsAC