Canonical Allele Identifier: CA2975981904

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027765_119027766del , CM000673.2:g.119027765_119027766del	GRCh38
NC_000011.9:g.118898475_118898476del , CM000673.1:g.118898475_118898476del	GRCh37
NC_000011.8:g.118403685_118403686del	NCBI36
NG_013331.1:g.8142_8143del , LRG_187:g.8142_8143del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.718_719del
ENST00000697845.1:n.642_643del
ENST00000697846.1:n.718_719del
ENST00000697847.1:n.718_719del
ENST00000697848.1:n.718_719del
ENST00000697849.1:n.1757_1758del
ENST00000697850.1:n.718_719del
ENST00000697851.1:n.2078_2079del
ENST00000638186.1:n.792_793del
ENST00000638360.1:n.624_625del
ENST00000638925.1:n.725_726del
ENST00000650539.1:n.894_895del
ENST00000330775.9:c.489_490del	ENSP00000476242.2:p.Tyr163Ter
ENST00000357590.9:c.489_490del	ENSP00000476176.2:p.Tyr163Ter
ENST00000524428.5:n.810_811del
ENST00000525039.5:n.912_913del
ENST00000525102.5:n.1246_1247del
ENST00000525372.5:n.489_490del
ENST00000526275.5:n.1270_1271del
ENST00000526626.6:n.451_452del
ENST00000527992.5:n.716_717del
ENST00000529510.5:n.399+429_399+430del
ENST00000530407.5:n.638_639del
ENST00000532085.1:n.3099_3100del
ENST00000532888.6:n.784_785del
ENST00000538950.5:c.270_271del	ENSP00000475991.2:p.Tyr90Ter
ENST00000545985.5:c.489_490del	ENSP00000475241.2:p.Tyr163Ter
NM_001164277.1:c.489_490del , LRG_187t1:c.489_490del	NP_001157749.1:p.Tyr163Ter
NM_001164278.1:c.489_490del	NP_001157750.1:p.Tyr163Ter
NM_001164279.1:c.270_271del	NP_001157751.1:p.Tyr90Ter
NM_001164280.1:c.489_490del	NP_001157752.1:p.Tyr163Ter
NM_001467.5:c.489_490del	NP_001458.1:p.Tyr163Ter
NM_001164278.2:c.489_490del	NP_001157750.1:p.Tyr163Ter
NM_001164279.2:c.270_271del	NP_001157751.1:p.Tyr90Ter
NM_001164280.2:c.489_490del	NP_001157752.1:p.Tyr163Ter
NM_001467.6:c.489_490del	NP_001458.1:p.Tyr163Ter
NM_001164277.2:c.489_490del MANE Select	NP_001157749.1:p.Tyr163Ter