Canonical Allele Identifier: CA2535046474

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025961_119025962del , CM000673.2:g.119025961_119025962del	GRCh38
NC_000011.9:g.118896671_118896672del , CM000673.1:g.118896671_118896672del	GRCh37
NC_000011.8:g.118401881_118401882del	NCBI36
NG_013331.1:g.9944_9945del , LRG_187:g.9944_9945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1128+5_1128+6del
ENST00000697845.1:n.1913_1914del
ENST00000697846.1:n.1128+5_1128+6del
ENST00000697847.1:n.1202-205_1202-204del
ENST00000697848.1:n.1214+5_1214+6del
ENST00000697849.1:n.3028_3029del
ENST00000697850.1:n.1219_1220del
ENST00000697851.1:n.2822+5_2822+6del
ENST00000638186.1:n.1288+5_1288+6del
ENST00000638360.1:n.1120+5_1120+6del
ENST00000638925.1:n.1253+5_1253+6del
ENST00000650539.1:n.1390+5_1390+6del
ENST00000330775.9:c.984+5_984+6del	ENSP00000476242.2:n.984+5_984+6del
ENST00000357590.9:c.984+5_984+6del	ENSP00000476176.2:n.984+5_984+6del
ENST00000524428.5:n.1220+5_1220+6del
ENST00000525039.5:n.1408+5_1408+6del
ENST00000525102.5:n.1742+5_1742+6del
ENST00000525372.5:n.1082+5_1082+6del
ENST00000526275.5:n.1766+5_1766+6del
ENST00000527992.5:n.1212+5_1212+6del
ENST00000529510.5:n.672+5_672+6del
ENST00000530407.5:n.1134+5_1134+6del
ENST00000532085.1:n.4370_4371del
ENST00000538950.5:c.765+5_765+6del	ENSP00000475991.2:n.765+5_765+6del
ENST00000545985.5:c.984+5_984+6del	ENSP00000475241.2:n.984+5_984+6del
NM_001164277.1:c.984+5_984+6del , LRG_187t1:c.984+5_984+6del	NP_001157749.1:n.984+5_984+6del
NM_001164278.1:c.984+5_984+6del	NP_001157750.1:n.984+5_984+6del
NM_001164279.1:c.765+5_765+6del	NP_001157751.1:n.765+5_765+6del
NM_001164280.1:c.984+5_984+6del	NP_001157752.1:n.984+5_984+6del
NM_001467.5:c.984+5_984+6del	NP_001458.1:n.984+5_984+6del
NM_001164278.2:c.984+5_984+6del	NP_001157750.1:n.984+5_984+6del
NM_001164279.2:c.765+5_765+6del	NP_001157751.1:n.765+5_765+6del
NM_001164280.2:c.984+5_984+6del	NP_001157752.1:n.984+5_984+6del
NM_001467.6:c.984+5_984+6del	NP_001458.1:n.984+5_984+6del
NM_001164277.2:c.984+5_984+6del MANE Select	NP_001157749.1:n.984+5_984+6del