Canonical Allele Identifier: CA2616339734
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025484A>G , CM000673.2:g.119025484A>G GRCh38
NC_000011.9:g.118896194A>G , CM000673.1:g.118896194A>G GRCh37
NC_000011.8:g.118401404A>G NCBI36
NG_013331.1:g.10422T>C , LRG_187:g.10422T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1195-155T>C
ENST00000697845.1:n.2184-155T>C
ENST00000697846.1:n.1402T>C
ENST00000697847.1:n.1268-155T>C
ENST00000697848.1:n.1488T>C
ENST00000697849.1:n.3506T>C
ENST00000697850.1:n.1697T>C
ENST00000697851.1:n.2823-155T>C
ENST00000638186.1:n.1289-155T>C
ENST00000638360.1:n.1121-155T>C
ENST00000638925.1:n.1254-155T>C
ENST00000650539.1:n.1457-155T>C
ENST00000330775.9:c.985-155T>C ENSP00000476242.2:n.985-155T>C
ENST00000357590.9:c.1051-155T>C ENSP00000476176.2:n.1051-155T>C
ENST00000524428.5:n.1221-155T>C
ENST00000525039.5:n.1475-155T>C
ENST00000525102.5:n.1743-155T>C
ENST00000525372.5:n.1083-155T>C
ENST00000526275.5:n.1767-155T>C
ENST00000527992.5:n.1213-155T>C
ENST00000529510.5:n.673-155T>C
ENST00000530407.5:n.1135-155T>C
ENST00000532085.1:n.4848T>C
ENST00000538950.5:c.766-155T>C ENSP00000475991.2:n.766-155T>C
ENST00000545985.5:c.985-155T>C ENSP00000475241.2:n.985-155T>C
NM_001164277.1:c.985-155T>C , LRG_187t1:c.985-155T>C NP_001157749.1:n.985-155T>C
NM_001164278.1:c.1051-155T>C NP_001157750.1:n.1051-155T>C
NM_001164279.1:c.766-155T>C NP_001157751.1:n.766-155T>C
NM_001164280.1:c.985-155T>C NP_001157752.1:n.985-155T>C
NM_001467.5:c.985-155T>C NP_001458.1:n.985-155T>C
NM_001164278.2:c.1051-155T>C NP_001157750.1:n.1051-155T>C
NM_001164279.2:c.766-155T>C NP_001157751.1:n.766-155T>C
NM_001164280.2:c.985-155T>C NP_001157752.1:n.985-155T>C
NM_001467.6:c.985-155T>C NP_001458.1:n.985-155T>C
NM_001164277.2:c.985-155T>C MANE Select NP_001157749.1:n.985-155T>C