Canonical Allele Identifier: CA2616339735
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025485A>C , CM000673.2:g.119025485A>C GRCh38
NC_000011.9:g.118896195A>C , CM000673.1:g.118896195A>C GRCh37
NC_000011.8:g.118401405A>C NCBI36
NG_013331.1:g.10421T>G , LRG_187:g.10421T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1195-156T>G
ENST00000697845.1:n.2184-156T>G
ENST00000697846.1:n.1401T>G
ENST00000697847.1:n.1268-156T>G
ENST00000697848.1:n.1487T>G
ENST00000697849.1:n.3505T>G
ENST00000697850.1:n.1696T>G
ENST00000697851.1:n.2823-156T>G
ENST00000638186.1:n.1289-156T>G
ENST00000638360.1:n.1121-156T>G
ENST00000638925.1:n.1254-156T>G
ENST00000650539.1:n.1457-156T>G
ENST00000330775.9:c.985-156T>G ENSP00000476242.2:n.985-156T>G
ENST00000357590.9:c.1051-156T>G ENSP00000476176.2:n.1051-156T>G
ENST00000524428.5:n.1221-156T>G
ENST00000525039.5:n.1475-156T>G
ENST00000525102.5:n.1743-156T>G
ENST00000525372.5:n.1083-156T>G
ENST00000526275.5:n.1767-156T>G
ENST00000527992.5:n.1213-156T>G
ENST00000529510.5:n.673-156T>G
ENST00000530407.5:n.1135-156T>G
ENST00000532085.1:n.4847T>G
ENST00000538950.5:c.766-156T>G ENSP00000475991.2:n.766-156T>G
ENST00000545985.5:c.985-156T>G ENSP00000475241.2:n.985-156T>G
NM_001164277.1:c.985-156T>G , LRG_187t1:c.985-156T>G NP_001157749.1:n.985-156T>G
NM_001164278.1:c.1051-156T>G NP_001157750.1:n.1051-156T>G
NM_001164279.1:c.766-156T>G NP_001157751.1:n.766-156T>G
NM_001164280.1:c.985-156T>G NP_001157752.1:n.985-156T>G
NM_001467.5:c.985-156T>G NP_001458.1:n.985-156T>G
NM_001164278.2:c.1051-156T>G NP_001157750.1:n.1051-156T>G
NM_001164279.2:c.766-156T>G NP_001157751.1:n.766-156T>G
NM_001164280.2:c.985-156T>G NP_001157752.1:n.985-156T>G
NM_001467.6:c.985-156T>G NP_001458.1:n.985-156T>G
NM_001164277.2:c.985-156T>G MANE Select NP_001157749.1:n.985-156T>G