Canonical Allele Identifier: CA672397959

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1326323500
• MyVariant Identifiers: chr11:g.118900688_118900689del (hg19) ; chr11:g.119029978_119029979del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029982_119029983del , CM000673.2:g.119029982_119029983del	GRCh38
NC_000011.9:g.118900692_118900693del , CM000673.1:g.118900692_118900693del	GRCh37
NC_000011.8:g.118405902_118405903del	NCBI36
NG_013331.1:g.5928_5929del , LRG_187:g.5928_5929del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-415_35-414del
ENST00000697846.1:n.35-415_35-414del
ENST00000697847.1:n.35-415_35-414del
ENST00000697848.1:n.35-415_35-414del
ENST00000697850.1:n.35-415_35-414del
ENST00000638360.1:n.43-415_43-414del
ENST00000638925.1:n.42-415_42-414del
ENST00000650539.1:n.210+191_210+192del
ENST00000330775.9:c.-195-415_-195-414del	ENSP00000476242.2:n.-195-415_-195-414del
ENST00000357590.9:c.-195-415_-195-414del	ENSP00000476176.2:n.-195-415_-195-414del
ENST00000525039.5:n.229-415_229-414del
ENST00000525102.5:n.562+253_562+254del
ENST00000527992.5:n.33-415_33-414del
ENST00000530407.5:n.25-415_25-414del
ENST00000532085.1:n.885_886del
ENST00000538950.5:c.-344-415_-344-414del	ENSP00000475991.2:n.-344-415_-344-414del
ENST00000545985.5:c.-196+253_-196+254del	ENSP00000475241.2:n.-196+253_-196+254del
NM_001164277.1:c.-196+253_-196+254del , LRG_187t1:c.-196+253_-196+254del	NP_001157749.1:n.-196+253_-196+254del
NM_001164278.1:c.-195-415_-195-414del	NP_001157750.1:n.-195-415_-195-414del
NM_001164279.1:c.-344-415_-344-414del	NP_001157751.1:n.-344-415_-344-414del
NM_001467.5:c.-195-415_-195-414del	NP_001458.1:n.-195-415_-195-414del
NM_001164278.2:c.-195-415_-195-414del	NP_001157750.1:n.-195-415_-195-414del
NM_001164279.2:c.-344-415_-344-414del	NP_001157751.1:n.-344-415_-344-414del
NM_001467.6:c.-195-415_-195-414del	NP_001458.1:n.-195-415_-195-414del
NM_001164277.2:c.-196+253_-196+254del MANE Select	NP_001157749.1:n.-196+253_-196+254del