Canonical Allele Identifier: CA2616334955

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026827-C-CTTTATT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026827_119026828insTTTATT , CM000673.2:g.119026827_119026828insTTTATT	GRCh38
NC_000011.9:g.118897537_118897538insTTTATT , CM000673.1:g.118897537_118897538insTTTATT	GRCh37
NC_000011.8:g.118402747_118402748insTTTATT	NCBI36
NG_013331.1:g.9078_9079insAATAAA , LRG_187:g.9078_9079insAATAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+109_1014+110insAATAAA
ENST00000697845.1:n.1047_1048insAATAAA
ENST00000697846.1:n.1014+109_1014+110insAATAAA
ENST00000697847.1:n.1014+109_1014+110insAATAAA
ENST00000697848.1:n.1014+109_1014+110insAATAAA
ENST00000697849.1:n.2162_2163insAATAAA
ENST00000697850.1:n.1014+109_1014+110insAATAAA
ENST00000697851.1:n.2483_2484insAATAAA
ENST00000638186.1:n.1088+109_1088+110insAATAAA
ENST00000638360.1:n.920+109_920+110insAATAAA
ENST00000638925.1:n.1021+109_1021+110insAATAAA
ENST00000650539.1:n.1190+109_1190+110insAATAAA
ENST00000330775.9:c.784+109_784+110insAATAAA	ENSP00000476242.2:n.784+109_784+110insAATAAA
ENST00000357590.9:c.784+109_784+110insAATAAA	ENSP00000476176.2:n.784+109_784+110insAATAAA
ENST00000524428.5:n.1106+109_1106+110insAATAAA
ENST00000525039.5:n.1208+109_1208+110insAATAAA
ENST00000525102.5:n.1542+109_1542+110insAATAAA
ENST00000525372.5:n.785+109_785+110insAATAAA
ENST00000526275.5:n.1566+109_1566+110insAATAAA
ENST00000527992.5:n.1012+109_1012+110insAATAAA
ENST00000529510.5:n.558+109_558+110insAATAAA
ENST00000530407.5:n.934+109_934+110insAATAAA
ENST00000532085.1:n.3504_3505insAATAAA
ENST00000532888.6:n.1189_1190insAATAAA
ENST00000538950.5:c.565+109_565+110insAATAAA	ENSP00000475991.2:n.565+109_565+110insAATAAA
ENST00000545985.5:c.784+109_784+110insAATAAA	ENSP00000475241.2:n.784+109_784+110insAATAAA
NM_001164277.1:c.784+109_784+110insAATAAA , LRG_187t1:c.784+109_784+110insAATAAA	NP_001157749.1:n.784+109_784+110insAATAAA
NM_001164278.1:c.784+109_784+110insAATAAA	NP_001157750.1:n.784+109_784+110insAATAAA
NM_001164279.1:c.565+109_565+110insAATAAA	NP_001157751.1:n.565+109_565+110insAATAAA
NM_001164280.1:c.784+109_784+110insAATAAA	NP_001157752.1:n.784+109_784+110insAATAAA
NM_001467.5:c.784+109_784+110insAATAAA	NP_001458.1:n.784+109_784+110insAATAAA
NM_001164278.2:c.784+109_784+110insAATAAA	NP_001157750.1:n.784+109_784+110insAATAAA
NM_001164279.2:c.565+109_565+110insAATAAA	NP_001157751.1:n.565+109_565+110insAATAAA
NM_001164280.2:c.784+109_784+110insAATAAA	NP_001157752.1:n.784+109_784+110insAATAAA
NM_001467.6:c.784+109_784+110insAATAAA	NP_001458.1:n.784+109_784+110insAATAAA
NM_001164277.2:c.784+109_784+110insAATAAA MANE Select	NP_001157749.1:n.784+109_784+110insAATAAA