Canonical Allele Identifier: CA2003775474

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029464_119029465delinsGT , CM000673.2:g.119029464_119029465delinsGT	GRCh38
NC_000011.9:g.118900174_118900175delinsGT , CM000673.1:g.118900174_118900175delinsGT	GRCh37
NC_000011.8:g.118405384_118405385delinsGT	NCBI36
NG_013331.1:g.6442_6443delinsAC , LRG_187:g.6442_6443delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.134_135delinsAC
ENST00000697846.1:n.134_135delinsAC
ENST00000697847.1:n.134_135delinsAC
ENST00000697848.1:n.134_135delinsAC
ENST00000697849.1:n.378_379delinsAC
ENST00000697850.1:n.134_135delinsAC
ENST00000697851.1:n.378_379delinsAC
ENST00000638186.1:n.208_209delinsAC
ENST00000638360.1:n.142_143delinsAC
ENST00000638925.1:n.141_142delinsAC
ENST00000650539.1:n.310_311delinsAC
ENST00000330775.9:c.-96_-95delinsAC	ENSP00000476242.2:n.-96_-95delinsAC
ENST00000357590.9:c.-96_-95delinsAC	ENSP00000476176.2:n.-96_-95delinsAC
ENST00000525039.5:n.328_329delinsAC
ENST00000525102.5:n.662_663delinsAC
ENST00000525787.1:n.200_201delinsAC
ENST00000526626.6:n.100_101delinsAC
ENST00000527992.5:n.132_133delinsAC
ENST00000530407.5:n.124_125delinsAC
ENST00000532085.1:n.1399_1400delinsAC
ENST00000532888.6:n.100_101delinsAC
ENST00000534384.1:n.125_126delinsAC
ENST00000538950.5:c.-245_-244delinsAC	ENSP00000475991.2:n.-245_-244delinsAC
ENST00000545985.5:c.-96_-95delinsAC	ENSP00000475241.2:n.-96_-95delinsAC
NM_001164277.1:c.-96_-95delinsAC , LRG_187t1:c.-96_-95delinsAC	NP_001157749.1:n.-96_-95delinsAC
NM_001164278.1:c.-96_-95delinsAC	NP_001157750.1:n.-96_-95delinsAC
NM_001164279.1:c.-245_-244delinsAC	NP_001157751.1:n.-245_-244delinsAC
NM_001164280.1:c.-96_-95delinsAC	NP_001157752.1:n.-96_-95delinsAC
NM_001467.5:c.-96_-95delinsAC	NP_001458.1:n.-96_-95delinsAC
NM_001164278.2:c.-96_-95delinsAC	NP_001157750.1:n.-96_-95delinsAC
NM_001164279.2:c.-245_-244delinsAC	NP_001157751.1:n.-245_-244delinsAC
NM_001164280.2:c.-96_-95delinsAC	NP_001157752.1:n.-96_-95delinsAC
NM_001467.6:c.-96_-95delinsAC	NP_001458.1:n.-96_-95delinsAC
NM_001164277.2:c.-96_-95delinsAC MANE Select	NP_001157749.1:n.-96_-95delinsAC