Canonical Allele Identifier: CA2003775348

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029390_119029391delinsAC , CM000673.2:g.119029390_119029391delinsAC	GRCh38
NC_000011.9:g.118900100_118900101delinsAC , CM000673.1:g.118900100_118900101delinsAC	GRCh37
NC_000011.8:g.118405310_118405311delinsAC	NCBI36
NG_013331.1:g.6516_6517delinsGT , LRG_187:g.6516_6517delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.208_209delinsGT
ENST00000697846.1:n.208_209delinsGT
ENST00000697847.1:n.208_209delinsGT
ENST00000697848.1:n.208_209delinsGT
ENST00000697849.1:n.452_453delinsGT
ENST00000697850.1:n.208_209delinsGT
ENST00000697851.1:n.452_453delinsGT
ENST00000638186.1:n.282_283delinsGT
ENST00000638360.1:n.216_217delinsGT
ENST00000638925.1:n.215_216delinsGT
ENST00000650539.1:n.384_385delinsGT
ENST00000330775.9:c.-22_-21delinsGT	ENSP00000476242.2:n.-22_-21delinsGT
ENST00000357590.9:c.-22_-21delinsGT	ENSP00000476176.2:n.-22_-21delinsGT
ENST00000525039.5:n.402_403delinsGT
ENST00000525102.5:n.736_737delinsGT
ENST00000525787.1:n.274_275delinsGT
ENST00000526626.6:n.174_175delinsGT
ENST00000527992.5:n.206_207delinsGT
ENST00000530407.5:n.197+1_197+2delinsGT
ENST00000532085.1:n.1473_1474delinsGT
ENST00000532888.6:n.174_175delinsGT
ENST00000534384.1:n.199_200delinsGT
ENST00000538950.5:c.-172+1_-172+2delinsGT	ENSP00000475991.2:n.-172+1_-172+2delinsGT...
ENST00000545985.5:c.-22_-21delinsGT	ENSP00000475241.2:n.-22_-21delinsGT
NM_001164277.1:c.-22_-21delinsGT , LRG_187t1:c.-22_-21delinsGT	NP_001157749.1:n.-22_-21delinsGT
NM_001164278.1:c.-22_-21delinsGT	NP_001157750.1:n.-22_-21delinsGT
NM_001164279.1:c.-172+1_-172+2delinsGT	NP_001157751.1:n.-172+1_-172+2delinsGT
NM_001164280.1:c.-22_-21delinsGT	NP_001157752.1:n.-22_-21delinsGT
NM_001467.5:c.-22_-21delinsGT	NP_001458.1:n.-22_-21delinsGT
NM_001164278.2:c.-22_-21delinsGT	NP_001157750.1:n.-22_-21delinsGT
NM_001164279.2:c.-172+1_-172+2delinsGT	NP_001157751.1:n.-172+1_-172+2delinsGT
NM_001164280.2:c.-22_-21delinsGT	NP_001157752.1:n.-22_-21delinsGT
NM_001467.6:c.-22_-21delinsGT	NP_001458.1:n.-22_-21delinsGT
NM_001164277.2:c.-22_-21delinsGT MANE Select	NP_001157749.1:n.-22_-21delinsGT