Canonical Allele Identifier: CA2003775629

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943688237

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029578_119029582del , CM000673.2:g.119029578_119029582del	GRCh38
NC_000011.9:g.118900288_118900292del , CM000673.1:g.118900288_118900292del	GRCh37
NC_000011.8:g.118405498_118405502del	NCBI36
NG_013331.1:g.6327_6331del , LRG_187:g.6327_6331del

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.35-16_35-12del
ENST00000697846.1:n.35-16_35-12del
ENST00000697847.1:n.35-16_35-12del
ENST00000697848.1:n.35-16_35-12del
ENST00000697849.1:n.263_267del
ENST00000697850.1:n.35-16_35-12del
ENST00000697851.1:n.263_267del
ENST00000638186.1:n.109-16_109-12del
ENST00000638360.1:n.43-16_43-12del
ENST00000638925.1:n.42-16_42-12del
ENST00000650539.1:n.211-16_211-12del
ENST00000330775.9:c.-195-16_-195-12del	ENSP00000476242.2:n.-195-16_-195-12del
ENST00000357590.9:c.-195-16_-195-12del	ENSP00000476176.2:n.-195-16_-195-12del
ENST00000525039.5:n.229-16_229-12del
ENST00000525102.5:n.563-16_563-12del
ENST00000525787.1:n.85_89del
ENST00000527992.5:n.33-16_33-12del
ENST00000530407.5:n.25-16_25-12del
ENST00000532085.1:n.1284_1288del
ENST00000534384.1:n.26-16_26-12del
ENST00000538950.5:c.-344-16_-344-12del	ENSP00000475991.2:n.-344-16_-344-12del
ENST00000545985.5:c.-195-16_-195-12del	ENSP00000475241.2:n.-195-16_-195-12del
NM_001164277.1:c.-195-16_-195-12del , LRG_187t1:c.-195-16_-195-12del	NP_001157749.1:n.-195-16_-195-12del
NM_001164278.1:c.-195-16_-195-12del	NP_001157750.1:n.-195-16_-195-12del
NM_001164279.1:c.-344-16_-344-12del	NP_001157751.1:n.-344-16_-344-12del
NM_001467.5:c.-195-16_-195-12del	NP_001458.1:n.-195-16_-195-12del
NM_001164278.2:c.-195-16_-195-12del	NP_001157750.1:n.-195-16_-195-12del
NM_001164279.2:c.-344-16_-344-12del	NP_001157751.1:n.-344-16_-344-12del
NM_001467.6:c.-195-16_-195-12del	NP_001458.1:n.-195-16_-195-12del
NM_001164277.2:c.-195-16_-195-12del MANE Select	NP_001157749.1:n.-195-16_-195-12del