Canonical Allele Identifier: CA2003748687

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025774_119025795delinsAAGAAAAGAAAACCAGGCCCAG , CM000673.2:g.119025774_119025795delinsAAGAAAAGAAAACCAGGCCCAG	GRCh38
NC_000011.9:g.118896484_118896505delinsAAGAAAAGAAAACCAGGCCCAG , CM000673.1:g.118896484_118896505delinsAAGAAAAGAAAACCAGGCCCAG	GRCh37
NC_000011.8:g.118401694_118401715delinsAAGAAAAGAAAACCAGGCCCAG	NCBI36
NG_013331.1:g.10111_10132delinsCTGGGCCTGGTTTTCTTTTCTT , LRG_187:g.10111_10132delinsCTGGGCCTGGTTTTCTTTTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1129-38_1129-17delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000697845.1:n.2080_2101delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000697846.1:n.1129-38_1129-17delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000697847.1:n.1202-38_1202-17delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000697848.1:n.1215-38_1215-17delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000697849.1:n.3195_3216delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000697850.1:n.1386_1407delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000697851.1:n.2822+172_2822+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000638186.1:n.1288+172_1288+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000638360.1:n.1120+172_1120+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000638925.1:n.1253+172_1253+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000650539.1:n.1391-38_1391-17delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000330775.9:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT	ENSP00000476242.2:n.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTC...
ENST00000357590.9:c.985-38_985-17delinsCTGGGCCTGGTTTTCTTTTCTT	ENSP00000476176.2:n.985-38_985-17delinsCTGGGCCTGGTTTTCTTTTCTT...
ENST00000524428.5:n.1220+172_1220+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000525039.5:n.1409-38_1409-17delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000525102.5:n.1742+172_1742+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000525372.5:n.1082+172_1082+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000526275.5:n.1766+172_1766+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000527992.5:n.1212+172_1212+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000529510.5:n.672+172_672+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000530407.5:n.1134+172_1134+193delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000532085.1:n.4537_4558delinsCTGGGCCTGGTTTTCTTTTCTT
ENST00000538950.5:c.765+172_765+193delinsCTGGGCCTGGTTTTCTTTTCTT	ENSP00000475991.2:n.765+172_765+193delinsCTGGGCCTGGTTTTCTTTTC...
ENST00000545985.5:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT	ENSP00000475241.2:n.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTC...
NM_001164277.1:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT , LRG_187t1:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001157749.1:n.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001164278.1:c.985-38_985-17delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001157750.1:n.985-38_985-17delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001164279.1:c.765+172_765+193delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001157751.1:n.765+172_765+193delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001164280.1:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001157752.1:n.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001467.5:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001458.1:n.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001164278.2:c.985-38_985-17delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001157750.1:n.985-38_985-17delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001164279.2:c.765+172_765+193delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001157751.1:n.765+172_765+193delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001164280.2:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001157752.1:n.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001467.6:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT	NP_001458.1:n.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT
NM_001164277.2:c.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT MANE Select	NP_001157749.1:n.984+172_984+193delinsCTGGGCCTGGTTTTCTTTTCTT