Canonical Allele Identifier: CA2975981872

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027756_119027758del , CM000673.2:g.119027756_119027758del	GRCh38
NC_000011.9:g.118898466_118898468del , CM000673.1:g.118898466_118898468del	GRCh37
NC_000011.8:g.118403676_118403678del	NCBI36
NG_013331.1:g.8149_8151del , LRG_187:g.8149_8151del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.725_727del
ENST00000697845.1:n.649_651del
ENST00000697846.1:n.725_727del
ENST00000697847.1:n.725_727del
ENST00000697848.1:n.725_727del
ENST00000697849.1:n.1764_1766del
ENST00000697850.1:n.725_727del
ENST00000697851.1:n.2085_2087del
ENST00000638186.1:n.799_801del
ENST00000638360.1:n.631_633del
ENST00000638925.1:n.732_734del
ENST00000650539.1:n.901_903del
ENST00000330775.9:c.496_498del	ENSP00000476242.2:p.Arg166del
ENST00000357590.9:c.496_498del	ENSP00000476176.2:p.Arg166del
ENST00000524428.5:n.817_819del
ENST00000525039.5:n.919_921del
ENST00000525102.5:n.1253_1255del
ENST00000525372.5:n.496_498del
ENST00000526275.5:n.1277_1279del
ENST00000526626.6:n.458_460del
ENST00000527992.5:n.723_725del
ENST00000529510.5:n.399+436_399+438del
ENST00000530407.5:n.645_647del
ENST00000532085.1:n.3106_3108del
ENST00000532888.6:n.791_793del
ENST00000538950.5:c.277_279del	ENSP00000475991.2:p.Arg93del
ENST00000545985.5:c.496_498del	ENSP00000475241.2:p.Arg166del
NM_001164277.1:c.496_498del , LRG_187t1:c.496_498del	NP_001157749.1:p.Arg166del
NM_001164278.1:c.496_498del	NP_001157750.1:p.Arg166del
NM_001164279.1:c.277_279del	NP_001157751.1:p.Arg93del
NM_001164280.1:c.496_498del	NP_001157752.1:p.Arg166del
NM_001467.5:c.496_498del	NP_001458.1:p.Arg166del
NM_001164278.2:c.496_498del	NP_001157750.1:p.Arg166del
NM_001164279.2:c.277_279del	NP_001157751.1:p.Arg93del
NM_001164280.2:c.496_498del	NP_001157752.1:p.Arg166del
NM_001467.6:c.496_498del	NP_001458.1:p.Arg166del
NM_001164277.2:c.496_498del MANE Select	NP_001157749.1:p.Arg166del