Canonical Allele Identifier: CA2003749352
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027044_119027045delinsAG , CM000673.2:g.119027044_119027045delinsAG GRCh38
NC_000011.9:g.118897754_118897755delinsAG , CM000673.1:g.118897754_118897755delinsAG GRCh37
NC_000011.8:g.118402964_118402965delinsAG NCBI36
NG_013331.1:g.8861_8862delinsCT , LRG_187:g.8861_8862delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.906_907delinsCT
ENST00000697845.1:n.830_831delinsCT
ENST00000697846.1:n.906_907delinsCT
ENST00000697847.1:n.906_907delinsCT
ENST00000697848.1:n.906_907delinsCT
ENST00000697849.1:n.1945_1946delinsCT
ENST00000697850.1:n.906_907delinsCT
ENST00000697851.1:n.2266_2267delinsCT
ENST00000638186.1:n.980_981delinsCT
ENST00000638360.1:n.812_813delinsCT
ENST00000638925.1:n.913_914delinsCT
ENST00000650539.1:n.1082_1083delinsCT
ENST00000330775.9:c.676_677delinsCT ENSP00000476242.2:p.Leu226=
ENST00000357590.9:c.676_677delinsCT ENSP00000476176.2:p.Leu226=
ENST00000524428.5:n.998_999delinsCT
ENST00000525039.5:n.1100_1101delinsCT
ENST00000525102.5:n.1434_1435delinsCT
ENST00000525372.5:n.677_678delinsCT
ENST00000526275.5:n.1458_1459delinsCT
ENST00000526626.6:n.639_640delinsCT
ENST00000527992.5:n.904_905delinsCT
ENST00000529510.5:n.450_451delinsCT
ENST00000530407.5:n.826_827delinsCT
ENST00000532085.1:n.3287_3288delinsCT
ENST00000532888.6:n.972_973delinsCT
ENST00000538950.5:c.457_458delinsCT ENSP00000475991.2:p.Leu153=
ENST00000545985.5:c.676_677delinsCT ENSP00000475241.2:p.Leu226=
NM_001164277.1:c.676_677delinsCT , LRG_187t1:c.676_677delinsCT NP_001157749.1:p.Leu226=
NM_001164278.1:c.676_677delinsCT NP_001157750.1:p.Leu226=
NM_001164279.1:c.457_458delinsCT NP_001157751.1:p.Leu153=
NM_001164280.1:c.676_677delinsCT NP_001157752.1:p.Leu226=
NM_001467.5:c.676_677delinsCT NP_001458.1:p.Leu226=
NM_001164278.2:c.676_677delinsCT NP_001157750.1:p.Leu226=
NM_001164279.2:c.457_458delinsCT NP_001157751.1:p.Leu153=
NM_001164280.2:c.676_677delinsCT NP_001157752.1:p.Leu226=
NM_001467.6:c.676_677delinsCT NP_001458.1:p.Leu226=
NM_001164277.2:c.676_677delinsCT MANE Select NP_001157749.1:p.Leu226=