Canonical Allele Identifier: CA2003748427
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025270_119025272delinsCAG , CM000673.2:g.119025270_119025272delinsCAG GRCh38
NC_000011.9:g.118895980_118895982delinsCAG , CM000673.1:g.118895980_118895982delinsCAG GRCh37
NC_000011.8:g.118401190_118401192delinsCAG NCBI36
NG_013331.1:g.10634_10636delinsCTG , LRG_187:g.10634_10636delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1252_1254delinsCTG (SLC37A4)
ENST00000697845.1:n.2241_2243delinsCTG (SLC37A4)
ENST00000697846.1:n.1614_1616delinsCTG (SLC37A4)
ENST00000697847.1:n.1325_1327delinsCTG (SLC37A4)
ENST00000697849.1:n.3718_3720delinsCTG (SLC37A4)
ENST00000697850.1:n.1909_1911delinsCTG (SLC37A4)
ENST00000697851.1:n.2880_2882delinsCTG (SLC37A4)
ENST00000638186.1:n.1346_1348delinsCTG (SLC37A4)
ENST00000638360.1:n.1178_1180delinsCTG (SLC37A4)
ENST00000638925.1:n.1311_1313delinsCTG (SLC37A4)
ENST00000650539.1:n.1514_1516delinsCTG (SLC37A4)
ENST00000330775.9:c.1042_1044delinsCTG (SLC37A4) ENSP00000476242.2:p.Leu348=
ENST00000357590.9:c.1108_1110delinsCTG (SLC37A4) ENSP00000476176.2:p.Leu370=
ENST00000524428.5:n.1278_1280delinsCTG (SLC37A4)
ENST00000525039.5:n.1532_1534delinsCTG (SLC37A4)
ENST00000525102.5:n.1800_1802delinsCTG (SLC37A4)
ENST00000525372.5:n.1140_1142delinsCTG (SLC37A4)
ENST00000526275.5:n.1824_1826delinsCTG (SLC37A4)
ENST00000527992.5:n.1270_1272delinsCTG (SLC37A4)
ENST00000529510.5:n.730_732delinsCTG (SLC37A4)
ENST00000530407.5:n.1192_1194delinsCTG (SLC37A4)
ENST00000532085.1:n.5060_5062delinsCTG (SLC37A4)
ENST00000533058.5:c.*221_*223delinsCAG (TRAPPC4) ENSP00000432920.1:n.*221_*223delinsCAG
ENST00000538950.5:c.823_825delinsCTG (SLC37A4) ENSP00000475991.2:p.Leu275=
ENST00000545985.5:c.1042_1044delinsCTG (SLC37A4) ENSP00000475241.2:p.Leu348=
NM_001164277.1:c.1042_1044delinsCTG , LRG_187t1:c.1042_1044delinsCTG (SLC37A4) NP_001157749.1:p.Leu348=
NM_001164278.1:c.1108_1110delinsCTG (SLC37A4) NP_001157750.1:p.Leu370=
NM_001164279.1:c.823_825delinsCTG (SLC37A4) NP_001157751.1:p.Leu275=
NM_001164280.1:c.1042_1044delinsCTG (SLC37A4) NP_001157752.1:p.Leu348=
NM_001467.5:c.1042_1044delinsCTG (SLC37A4) NP_001458.1:p.Leu348=
NM_001164278.2:c.1108_1110delinsCTG (SLC37A4) NP_001157750.1:p.Leu370=
NM_001164279.2:c.823_825delinsCTG (SLC37A4) NP_001157751.1:p.Leu275=
NM_001164280.2:c.1042_1044delinsCTG (SLC37A4) NP_001157752.1:p.Leu348=
NM_001467.6:c.1042_1044delinsCTG (SLC37A4) NP_001458.1:p.Leu348=
NM_001164277.2:c.1042_1044delinsCTG (SLC37A4) MANE Select NP_001157749.1:p.Leu348=