Canonical Allele Identifier: CA2003749315
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026966_119026967delinsAT , CM000673.2:g.119026966_119026967delinsAT GRCh38
NC_000011.9:g.118897676_118897677delinsAT , CM000673.1:g.118897676_118897677delinsAT GRCh37
NC_000011.8:g.118402886_118402887delinsAT NCBI36
NG_013331.1:g.8939_8940delinsAT , LRG_187:g.8939_8940delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.984_985delinsAT
ENST00000697845.1:n.908_909delinsAT
ENST00000697846.1:n.984_985delinsAT
ENST00000697847.1:n.984_985delinsAT
ENST00000697848.1:n.984_985delinsAT
ENST00000697849.1:n.2023_2024delinsAT
ENST00000697850.1:n.984_985delinsAT
ENST00000697851.1:n.2344_2345delinsAT
ENST00000638186.1:n.1058_1059delinsAT
ENST00000638360.1:n.890_891delinsAT
ENST00000638925.1:n.991_992delinsAT
ENST00000650539.1:n.1160_1161delinsAT
ENST00000330775.9:c.754_755delinsAT ENSP00000476242.2:p.Ile252=
ENST00000357590.9:c.754_755delinsAT ENSP00000476176.2:p.Ile252=
ENST00000524428.5:n.1076_1077delinsAT
ENST00000525039.5:n.1178_1179delinsAT
ENST00000525102.5:n.1512_1513delinsAT
ENST00000525372.5:n.755_756delinsAT
ENST00000526275.5:n.1536_1537delinsAT
ENST00000526626.6:n.717_718delinsAT
ENST00000527992.5:n.982_983delinsAT
ENST00000529510.5:n.528_529delinsAT
ENST00000530407.5:n.904_905delinsAT
ENST00000532085.1:n.3365_3366delinsAT
ENST00000532888.6:n.1050_1051delinsAT
ENST00000538950.5:c.535_536delinsAT ENSP00000475991.2:p.Ile179=
ENST00000545985.5:c.754_755delinsAT ENSP00000475241.2:p.Ile252=
NM_001164277.1:c.754_755delinsAT , LRG_187t1:c.754_755delinsAT NP_001157749.1:p.Ile252=
NM_001164278.1:c.754_755delinsAT NP_001157750.1:p.Ile252=
NM_001164279.1:c.535_536delinsAT NP_001157751.1:p.Ile179=
NM_001164280.1:c.754_755delinsAT NP_001157752.1:p.Ile252=
NM_001467.5:c.754_755delinsAT NP_001458.1:p.Ile252=
NM_001164278.2:c.754_755delinsAT NP_001157750.1:p.Ile252=
NM_001164279.2:c.535_536delinsAT NP_001157751.1:p.Ile179=
NM_001164280.2:c.754_755delinsAT NP_001157752.1:p.Ile252=
NM_001467.6:c.754_755delinsAT NP_001458.1:p.Ile252=
NM_001164277.2:c.754_755delinsAT MANE Select NP_001157749.1:p.Ile252=