Canonical Allele Identifier: CA918979957

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1555192055

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119030022_119030023delinsAT , CM000673.2:g.119030022_119030023delinsAT	GRCh38
NC_000011.9:g.118900732_118900733delinsAT , CM000673.1:g.118900732_118900733delinsAT	GRCh37
NC_000011.8:g.118405942_118405943delinsAT	NCBI36
NG_013331.1:g.5884_5885delinsAT , LRG_187:g.5884_5885delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-459_35-458delinsAT
ENST00000697846.1:n.35-459_35-458delinsAT
ENST00000697847.1:n.35-459_35-458delinsAT
ENST00000697848.1:n.35-459_35-458delinsAT
ENST00000697850.1:n.35-459_35-458delinsAT
ENST00000638360.1:n.43-459_43-458delinsAT
ENST00000638925.1:n.42-459_42-458delinsAT
ENST00000650539.1:n.210+147_210+148delinsAT
ENST00000330775.9:c.-195-459_-195-458delinsAT	ENSP00000476242.2:n.-195-459_-195-458delinsAT
ENST00000357590.9:c.-195-459_-195-458delinsAT	ENSP00000476176.2:n.-195-459_-195-458delinsAT
ENST00000525039.5:n.229-459_229-458delinsAT
ENST00000525102.5:n.562+209_562+210delinsAT
ENST00000527992.5:n.33-459_33-458delinsAT
ENST00000530407.5:n.25-459_25-458delinsAT
ENST00000532085.1:n.841_842delinsAT
ENST00000538950.5:c.-344-459_-344-458delinsAT	ENSP00000475991.2:n.-344-459_-344-458delinsAT
ENST00000545985.5:c.-196+209_-196+210delinsAT	ENSP00000475241.2:n.-196+209_-196+210delinsAT
NM_001164277.1:c.-196+209_-196+210delinsAT , LRG_187t1:c.-196+209_-196+210delinsAT	NP_001157749.1:n.-196+209_-196+210delinsAT
NM_001164278.1:c.-195-459_-195-458delinsAT	NP_001157750.1:n.-195-459_-195-458delinsAT
NM_001164279.1:c.-344-459_-344-458delinsAT	NP_001157751.1:n.-344-459_-344-458delinsAT
NM_001467.5:c.-195-459_-195-458delinsAT	NP_001458.1:n.-195-459_-195-458delinsAT
NM_001164278.2:c.-195-459_-195-458delinsAT	NP_001157750.1:n.-195-459_-195-458delinsAT
NM_001164279.2:c.-344-459_-344-458delinsAT	NP_001157751.1:n.-344-459_-344-458delinsAT
NM_001467.6:c.-195-459_-195-458delinsAT	NP_001458.1:n.-195-459_-195-458delinsAT
NM_001164277.2:c.-196+209_-196+210delinsAT MANE Select	NP_001157749.1:n.-196+209_-196+210delinsAT