Canonical Allele Identifier: CA2689944744

Gene: GNE CLTA

Linked Data

• gnomAD v4: 9-36219690-AGTTTTAGTGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36219692_36219701del , CM000671.2:g.36219692_36219701del	GRCh38
NC_000009.11:g.36219689_36219698del , CM000671.1:g.36219689_36219698del	GRCh37
NC_000009.10:g.36209689_36209698del	NCBI36
NG_008246.1:g.62345_62354del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1909+138_1909+147del (GNE) MANE Plus Clinical	ENSP00000379839.3:n.1909+138_1909+147del
ENST00000543356.7:c.1639+138_1639+147del (GNE)	ENSP00000437765.3:n.1639+138_1639+147del
ENST00000642385.2:c.1816+138_1816+147del (GNE) MANE Select	ENSP00000494141.2:n.1816+138_1816+147del
ENST00000377902.5:c.1816+138_1816+147del (GNE)	ENSP00000367134.4:n.1816+138_1816+147del
ENST00000396594.7:c.1909+138_1909+147del (GNE)	ENSP00000379839.3:n.1909+138_1909+147del
ENST00000447283.6:c.1594+138_1594+147del (GNE)	ENSP00000414760.2:n.1594+138_1594+147del
ENST00000464497.5:c.485+15513_485+15522del (CLTA)	ENSP00000419158.1:n.485+15513_485+15522del
ENST00000539208.5:c.1486+138_1486+147del (GNE)	ENSP00000445117.1:n.1486+138_1486+147del
ENST00000539815.5:c.1816+138_1816+147del (GNE)	ENSP00000439155.1:n.1816+138_1816+147del
ENST00000543356.6:c.1801+138_1801+147del (GNE)	ENSP00000437765.2:n.1801+138_1801+147del
NM_001128227.2:c.1909+138_1909+147del (GNE)	NP_001121699.1:n.1909+138_1909+147del
NM_001190383.1:c.1594+138_1594+147del (GNE)	NP_001177312.1:n.1594+138_1594+147del
NM_001190384.1:c.1486+138_1486+147del (GNE)	NP_001177313.1:n.1486+138_1486+147del
NM_001190388.1:c.1801+138_1801+147del (GNE)	NP_001177317.1:n.1801+138_1801+147del
NM_005476.5:c.1816+138_1816+147del (GNE)	NP_005467.1:n.1816+138_1816+147del
XM_005251334.3:c.1756+138_1756+147del (GNE)	XP_005251391.1:n.1756+138_1756+147del
NM_001190383.2:c.1594+138_1594+147del (GNE)	NP_001177312.1:n.1594+138_1594+147del
NM_001190384.2:c.1486+138_1486+147del (GNE)	NP_001177313.1:n.1486+138_1486+147del
NM_005476.6:c.1816+138_1816+147del (GNE)	NP_005467.1:n.1816+138_1816+147del
XM_005251334.4:c.1756+138_1756+147del (GNE)	XP_005251391.1:n.1756+138_1756+147del
XM_017014167.1:c.1816+138_1816+147del (GNE)	XP_016869656.1:n.1816+138_1816+147del
XM_017014168.1:c.1663+138_1663+147del (GNE)	XP_016869657.1:n.1663+138_1663+147del
NM_001128227.3:c.1909+138_1909+147del (GNE) MANE Plus Clinical	NP_001121699.1:n.1909+138_1909+147del
NM_001190383.3:c.1594+138_1594+147del (GNE)	NP_001177312.1:n.1594+138_1594+147del
NM_001190384.3:c.1486+138_1486+147del (GNE)	NP_001177313.1:n.1486+138_1486+147del
NM_001190388.2:c.1639+138_1639+147del (GNE)	NP_001177317.2:n.1639+138_1639+147del
NM_001374797.1:c.1663+138_1663+147del (GNE)	NP_001361726.1:n.1663+138_1663+147del
NM_001374798.1:c.1639+138_1639+147del (GNE)	NP_001361727.1:n.1639+138_1639+147del
NM_005476.7:c.1816+138_1816+147del (GNE) MANE Select	NP_005467.1:n.1816+138_1816+147del