Canonical Allele Identifier: CA2003749263
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026880_119026881delinsAT , CM000673.2:g.119026880_119026881delinsAT GRCh38
NC_000011.9:g.118897590_118897591delinsAT , CM000673.1:g.118897590_118897591delinsAT GRCh37
NC_000011.8:g.118402800_118402801delinsAT NCBI36
NG_013331.1:g.9025_9026delinsAT , LRG_187:g.9025_9026delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1014+56_1014+57delinsAT
ENST00000697845.1:n.994_995delinsAT
ENST00000697846.1:n.1014+56_1014+57delinsAT
ENST00000697847.1:n.1014+56_1014+57delinsAT
ENST00000697848.1:n.1014+56_1014+57delinsAT
ENST00000697849.1:n.2109_2110delinsAT
ENST00000697850.1:n.1014+56_1014+57delinsAT
ENST00000697851.1:n.2430_2431delinsAT
ENST00000638186.1:n.1088+56_1088+57delinsAT
ENST00000638360.1:n.920+56_920+57delinsAT
ENST00000638925.1:n.1021+56_1021+57delinsAT
ENST00000650539.1:n.1190+56_1190+57delinsAT
ENST00000330775.9:c.784+56_784+57delinsAT ENSP00000476242.2:n.784+56_784+57delinsAT
ENST00000357590.9:c.784+56_784+57delinsAT ENSP00000476176.2:n.784+56_784+57delinsAT
ENST00000524428.5:n.1106+56_1106+57delinsAT
ENST00000525039.5:n.1208+56_1208+57delinsAT
ENST00000525102.5:n.1542+56_1542+57delinsAT
ENST00000525372.5:n.785+56_785+57delinsAT
ENST00000526275.5:n.1566+56_1566+57delinsAT
ENST00000527992.5:n.1012+56_1012+57delinsAT
ENST00000529510.5:n.558+56_558+57delinsAT
ENST00000530407.5:n.934+56_934+57delinsAT
ENST00000532085.1:n.3451_3452delinsAT
ENST00000532888.6:n.1136_1137delinsAT
ENST00000538950.5:c.565+56_565+57delinsAT ENSP00000475991.2:n.565+56_565+57delinsAT
ENST00000545985.5:c.784+56_784+57delinsAT ENSP00000475241.2:n.784+56_784+57delinsAT
NM_001164277.1:c.784+56_784+57delinsAT , LRG_187t1:c.784+56_784+57delinsAT NP_001157749.1:n.784+56_784+57delinsAT
NM_001164278.1:c.784+56_784+57delinsAT NP_001157750.1:n.784+56_784+57delinsAT
NM_001164279.1:c.565+56_565+57delinsAT NP_001157751.1:n.565+56_565+57delinsAT
NM_001164280.1:c.784+56_784+57delinsAT NP_001157752.1:n.784+56_784+57delinsAT
NM_001467.5:c.784+56_784+57delinsAT NP_001458.1:n.784+56_784+57delinsAT
NM_001164278.2:c.784+56_784+57delinsAT NP_001157750.1:n.784+56_784+57delinsAT
NM_001164279.2:c.565+56_565+57delinsAT NP_001157751.1:n.565+56_565+57delinsAT
NM_001164280.2:c.784+56_784+57delinsAT NP_001157752.1:n.784+56_784+57delinsAT
NM_001467.6:c.784+56_784+57delinsAT NP_001458.1:n.784+56_784+57delinsAT
NM_001164277.2:c.784+56_784+57delinsAT MANE Select NP_001157749.1:n.784+56_784+57delinsAT