Canonical Allele Identifier: CA2003749691
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027719_119027724delinsAACCAC , CM000673.2:g.119027719_119027724delinsAACCAC GRCh38
NC_000011.9:g.118898429_118898434delinsAACCAC , CM000673.1:g.118898429_118898434delinsAACCAC GRCh37
NC_000011.8:g.118403639_118403644delinsAACCAC NCBI36
NG_013331.1:g.8182_8187delinsGTGGTT , LRG_187:g.8182_8187delinsGTGGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.759_764delinsGTGGTT
ENST00000697845.1:n.683_688delinsGTGGTT
ENST00000697846.1:n.759_764delinsGTGGTT
ENST00000697847.1:n.759_764delinsGTGGTT
ENST00000697848.1:n.759_764delinsGTGGTT
ENST00000697849.1:n.1798_1803delinsGTGGTT
ENST00000697850.1:n.759_764delinsGTGGTT
ENST00000697851.1:n.2119_2124delinsGTGGTT
ENST00000638186.1:n.833_838delinsGTGGTT
ENST00000638360.1:n.665_670delinsGTGGTT
ENST00000638925.1:n.766_771delinsGTGGTT
ENST00000650539.1:n.935_940delinsGTGGTT
ENST00000330775.9:c.529_534delinsGTGGTT ENSP00000476242.2:p.Val177=
ENST00000357590.9:c.529_534delinsGTGGTT ENSP00000476176.2:p.Val177=
ENST00000524428.5:n.851_856delinsGTGGTT
ENST00000525039.5:n.953_958delinsGTGGTT
ENST00000525102.5:n.1287_1292delinsGTGGTT
ENST00000525372.5:n.530_535delinsGTGGTT
ENST00000526275.5:n.1311_1316delinsGTGGTT
ENST00000526626.6:n.492_497delinsGTGGTT
ENST00000527992.5:n.757_762delinsGTGGTT
ENST00000529510.5:n.399+470_399+475delinsGTGGTT
ENST00000530407.5:n.679_684delinsGTGGTT
ENST00000532085.1:n.3140_3145delinsGTGGTT
ENST00000532888.6:n.825_830delinsGTGGTT
ENST00000538950.5:c.310_315delinsGTGGTT ENSP00000475991.2:p.Val104=
ENST00000545985.5:c.529_534delinsGTGGTT ENSP00000475241.2:p.Val177=
NM_001164277.1:c.529_534delinsGTGGTT , LRG_187t1:c.529_534delinsGTGGTT NP_001157749.1:p.Val177=
NM_001164278.1:c.529_534delinsGTGGTT NP_001157750.1:p.Val177=
NM_001164279.1:c.310_315delinsGTGGTT NP_001157751.1:p.Val104=
NM_001164280.1:c.529_534delinsGTGGTT NP_001157752.1:p.Val177=
NM_001467.5:c.529_534delinsGTGGTT NP_001458.1:p.Val177=
NM_001164278.2:c.529_534delinsGTGGTT NP_001157750.1:p.Val177=
NM_001164279.2:c.310_315delinsGTGGTT NP_001157751.1:p.Val104=
NM_001164280.2:c.529_534delinsGTGGTT NP_001157752.1:p.Val177=
NM_001467.6:c.529_534delinsGTGGTT NP_001458.1:p.Val177=
NM_001164277.2:c.529_534delinsGTGGTT MANE Select NP_001157749.1:p.Val177=