Canonical Allele Identifier: CA2003749761

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943621397

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027841_119027844del , CM000673.2:g.119027841_119027844del	GRCh38
NC_000011.9:g.118898551_118898554del , CM000673.1:g.118898551_118898554del	GRCh37
NC_000011.8:g.118403761_118403764del	NCBI36
NG_013331.1:g.8065_8068del , LRG_187:g.8065_8068del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.641_644del
ENST00000697845.1:n.565_568del
ENST00000697846.1:n.641_644del
ENST00000697847.1:n.641_644del
ENST00000697848.1:n.641_644del
ENST00000697849.1:n.1680_1683del
ENST00000697850.1:n.641_644del
ENST00000697851.1:n.2001_2004del
ENST00000638186.1:n.715_718del
ENST00000638360.1:n.619-72_619-69del
ENST00000638925.1:n.648_651del
ENST00000650539.1:n.817_820del
ENST00000330775.9:c.412_415del	ENSP00000476242.2:p.Trp138ProfsTer7
ENST00000357590.9:c.412_415del	ENSP00000476176.2:p.Trp138ProfsTer7
ENST00000524428.5:n.733_736del
ENST00000525039.5:n.835_838del
ENST00000525102.5:n.1169_1172del
ENST00000525372.5:n.412_415del
ENST00000525787.1:n.1028_1031del
ENST00000526275.5:n.1193_1196del
ENST00000526626.6:n.374_377del
ENST00000527992.5:n.639_642del
ENST00000529510.5:n.399+352_399+355del
ENST00000530407.5:n.561_564del
ENST00000532085.1:n.3022_3025del
ENST00000532888.6:n.707_710del
ENST00000538950.5:c.193_196del	ENSP00000475991.2:p.Trp65ProfsTer7
ENST00000545985.5:c.412_415del	ENSP00000475241.2:p.Trp138ProfsTer7
NM_001164277.1:c.412_415del , LRG_187t1:c.412_415del	NP_001157749.1:p.Trp138ProfsTer7
NM_001164278.1:c.412_415del	NP_001157750.1:p.Trp138ProfsTer7
NM_001164279.1:c.193_196del	NP_001157751.1:p.Trp65ProfsTer7
NM_001164280.1:c.412_415del	NP_001157752.1:p.Trp138ProfsTer7
NM_001467.5:c.412_415del	NP_001458.1:p.Trp138ProfsTer7
NM_001164278.2:c.412_415del	NP_001157750.1:p.Trp138ProfsTer7
NM_001164279.2:c.193_196del	NP_001157751.1:p.Trp65ProfsTer7
NM_001164280.2:c.412_415del	NP_001157752.1:p.Trp138ProfsTer7
NM_001467.6:c.412_415del	NP_001458.1:p.Trp138ProfsTer7
NM_001164277.2:c.412_415del MANE Select	NP_001157749.1:p.Trp138ProfsTer7