Canonical Allele Identifier: CA2003749267
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026882C= , CM000673.2:g.119026882C= GRCh38
NC_000011.9:g.118897592C= , CM000673.1:g.118897592C= GRCh37
NC_000011.8:g.118402802C= NCBI36
NG_013331.1:g.9024G= , LRG_187:g.9024G=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1014+55G=
ENST00000697845.1:n.993G=
ENST00000697846.1:n.1014+55G=
ENST00000697847.1:n.1014+55G=
ENST00000697848.1:n.1014+55G=
ENST00000697849.1:n.2108G=
ENST00000697850.1:n.1014+55G=
ENST00000697851.1:n.2429G=
ENST00000638186.1:n.1088+55G=
ENST00000638360.1:n.920+55G=
ENST00000638925.1:n.1021+55G=
ENST00000650539.1:n.1190+55G=
ENST00000330775.9:c.784+55G= ENSP00000476242.2:n.784+55G=
ENST00000357590.9:c.784+55G= ENSP00000476176.2:n.784+55G=
ENST00000524428.5:n.1106+55G=
ENST00000525039.5:n.1208+55G=
ENST00000525102.5:n.1542+55G=
ENST00000525372.5:n.785+55G=
ENST00000526275.5:n.1566+55G=
ENST00000527992.5:n.1012+55G=
ENST00000529510.5:n.558+55G=
ENST00000530407.5:n.934+55G=
ENST00000532085.1:n.3450G=
ENST00000532888.6:n.1135G=
ENST00000538950.5:c.565+55G= ENSP00000475991.2:n.565+55G=
ENST00000545985.5:c.784+55G= ENSP00000475241.2:n.784+55G=
NM_001164277.1:c.784+55G= , LRG_187t1:c.784+55G= NP_001157749.1:n.784+55G=
NM_001164278.1:c.784+55G= NP_001157750.1:n.784+55G=
NM_001164279.1:c.565+55G= NP_001157751.1:n.565+55G=
NM_001164280.1:c.784+55G= NP_001157752.1:n.784+55G=
NM_001467.5:c.784+55G= NP_001458.1:n.784+55G=
NM_001164278.2:c.784+55G= NP_001157750.1:n.784+55G=
NM_001164279.2:c.565+55G= NP_001157751.1:n.565+55G=
NM_001164280.2:c.784+55G= NP_001157752.1:n.784+55G=
NM_001467.6:c.784+55G= NP_001458.1:n.784+55G=
NM_001164277.2:c.784+55G= MANE Select NP_001157749.1:n.784+55G=