Canonical Allele Identifier: CA2003748439

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025285_119025286delinsAT , CM000673.2:g.119025285_119025286delinsAT	GRCh38
NC_000011.9:g.118895995_118895996delinsAT , CM000673.1:g.118895995_118895996delinsAT	GRCh37
NC_000011.8:g.118401205_118401206delinsAT	NCBI36
NG_013331.1:g.10620_10621delinsAT , LRG_187:g.10620_10621delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1238_1239delinsAT (SLC37A4)
ENST00000697845.1:n.2227_2228delinsAT (SLC37A4)
ENST00000697846.1:n.1600_1601delinsAT (SLC37A4)
ENST00000697847.1:n.1311_1312delinsAT (SLC37A4)
ENST00000697849.1:n.3704_3705delinsAT (SLC37A4)
ENST00000697850.1:n.1895_1896delinsAT (SLC37A4)
ENST00000697851.1:n.2866_2867delinsAT (SLC37A4)
ENST00000638186.1:n.1332_1333delinsAT (SLC37A4)
ENST00000638360.1:n.1164_1165delinsAT (SLC37A4)
ENST00000638925.1:n.1297_1298delinsAT (SLC37A4)
ENST00000650539.1:n.1500_1501delinsAT (SLC37A4)
ENST00000330775.9:c.1028_1029delinsAT (SLC37A4)	ENSP00000476242.2:p.Tyr343=
ENST00000357590.9:c.1094_1095delinsAT (SLC37A4)	ENSP00000476176.2:p.Tyr365=
ENST00000524428.5:n.1264_1265delinsAT (SLC37A4)
ENST00000525039.5:n.1518_1519delinsAT (SLC37A4)
ENST00000525102.5:n.1786_1787delinsAT (SLC37A4)
ENST00000525372.5:n.1126_1127delinsAT (SLC37A4)
ENST00000526275.5:n.1810_1811delinsAT (SLC37A4)
ENST00000527992.5:n.1256_1257delinsAT (SLC37A4)
ENST00000529510.5:n.716_717delinsAT (SLC37A4)
ENST00000530407.5:n.1178_1179delinsAT (SLC37A4)
ENST00000532085.1:n.5046_5047delinsAT (SLC37A4)
ENST00000533058.5:c.*236_*237delinsAT (TRAPPC4)	ENSP00000432920.1:n.*236_*237delinsAT
ENST00000538950.5:c.809_810delinsAT (SLC37A4)	ENSP00000475991.2:p.Tyr270=
ENST00000545985.5:c.1028_1029delinsAT (SLC37A4)	ENSP00000475241.2:p.Tyr343=
NM_001164277.1:c.1028_1029delinsAT , LRG_187t1:c.1028_1029delinsAT (SLC37A4)	NP_001157749.1:p.Tyr343=
NM_001164278.1:c.1094_1095delinsAT (SLC37A4)	NP_001157750.1:p.Tyr365=
NM_001164279.1:c.809_810delinsAT (SLC37A4)	NP_001157751.1:p.Tyr270=
NM_001164280.1:c.1028_1029delinsAT (SLC37A4)	NP_001157752.1:p.Tyr343=
NM_001467.5:c.1028_1029delinsAT (SLC37A4)	NP_001458.1:p.Tyr343=
NM_001164278.2:c.1094_1095delinsAT (SLC37A4)	NP_001157750.1:p.Tyr365=
NM_001164279.2:c.809_810delinsAT (SLC37A4)	NP_001157751.1:p.Tyr270=
NM_001164280.2:c.1028_1029delinsAT (SLC37A4)	NP_001157752.1:p.Tyr343=
NM_001467.6:c.1028_1029delinsAT (SLC37A4)	NP_001458.1:p.Tyr343=
NM_001164277.2:c.1028_1029delinsAT (SLC37A4) MANE Select	NP_001157749.1:p.Tyr343=