Canonical Allele Identifier: CA2003749654
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027657_119027658delinsAG , CM000673.2:g.119027657_119027658delinsAG GRCh38
NC_000011.9:g.118898367_118898368delinsAG , CM000673.1:g.118898367_118898368delinsAG GRCh37
NC_000011.8:g.118403577_118403578delinsAG NCBI36
NG_013331.1:g.8248_8249delinsCT , LRG_187:g.8248_8249delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.825_826delinsCT
ENST00000697845.1:n.749_750delinsCT
ENST00000697846.1:n.825_826delinsCT
ENST00000697847.1:n.825_826delinsCT
ENST00000697848.1:n.825_826delinsCT
ENST00000697849.1:n.1864_1865delinsCT
ENST00000697850.1:n.825_826delinsCT
ENST00000697851.1:n.2185_2186delinsCT
ENST00000638186.1:n.899_900delinsCT
ENST00000638360.1:n.731_732delinsCT
ENST00000638925.1:n.832_833delinsCT
ENST00000650539.1:n.1001_1002delinsCT
ENST00000330775.9:c.595_596delinsCT ENSP00000476242.2:p.Leu199=
ENST00000357590.9:c.595_596delinsCT ENSP00000476176.2:p.Leu199=
ENST00000524428.5:n.917_918delinsCT
ENST00000525039.5:n.1019_1020delinsCT
ENST00000525102.5:n.1353_1354delinsCT
ENST00000525372.5:n.596_597delinsCT
ENST00000526275.5:n.1377_1378delinsCT
ENST00000526626.6:n.558_559delinsCT
ENST00000527992.5:n.823_824delinsCT
ENST00000529510.5:n.399+536_399+537delinsCT
ENST00000530407.5:n.745_746delinsCT
ENST00000532085.1:n.3206_3207delinsCT
ENST00000532888.6:n.891_892delinsCT
ENST00000538950.5:c.376_377delinsCT ENSP00000475991.2:p.Leu126=
ENST00000545985.5:c.595_596delinsCT ENSP00000475241.2:p.Leu199=
NM_001164277.1:c.595_596delinsCT , LRG_187t1:c.595_596delinsCT NP_001157749.1:p.Leu199=
NM_001164278.1:c.595_596delinsCT NP_001157750.1:p.Leu199=
NM_001164279.1:c.376_377delinsCT NP_001157751.1:p.Leu126=
NM_001164280.1:c.595_596delinsCT NP_001157752.1:p.Leu199=
NM_001467.5:c.595_596delinsCT NP_001458.1:p.Leu199=
NM_001164278.2:c.595_596delinsCT NP_001157750.1:p.Leu199=
NM_001164279.2:c.376_377delinsCT NP_001157751.1:p.Leu126=
NM_001164280.2:c.595_596delinsCT NP_001157752.1:p.Leu199=
NM_001467.6:c.595_596delinsCT NP_001458.1:p.Leu199=
NM_001164277.2:c.595_596delinsCT MANE Select NP_001157749.1:p.Leu199=