Canonical Allele Identifier: CA382900216
Gene: SLC37A4 HGNC NCBI

Linked Data

dbSNP Id: rs1304042332

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026643C>G , CM000673.2:g.119026643C>G GRCh38
NC_000011.9:g.118897353C>G , CM000673.1:g.118897353C>G GRCh37
NC_000011.8:g.118402563C>G NCBI36
NG_013331.1:g.9263G>C , LRG_187:g.9263G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1014+294G>C
ENST00000697845.1:n.1232G>C
ENST00000697846.1:n.1014+294G>C
ENST00000697847.1:n.1060G>C
ENST00000697848.1:n.1060G>C
ENST00000697849.1:n.2347G>C
ENST00000697850.1:n.1060G>C
ENST00000697851.1:n.2668G>C
ENST00000638186.1:n.1134G>C
ENST00000638360.1:n.966G>C
ENST00000638925.1:n.1067G>C
ENST00000650539.1:n.1236G>C
ENST00000330775.9:c.830G>C ENSP00000476242.2:p.Ser277Thr
ENST00000357590.9:c.830G>C ENSP00000476176.2:p.Ser277Thr
ENST00000524428.5:n.1106+294G>C
ENST00000525039.5:n.1254G>C
ENST00000525102.5:n.1588G>C
ENST00000525372.5:n.831G>C
ENST00000526275.5:n.1612G>C
ENST00000527992.5:n.1058G>C
ENST00000529510.5:n.558+294G>C
ENST00000530407.5:n.980G>C
ENST00000532085.1:n.3689G>C
ENST00000538950.5:c.611G>C ENSP00000475991.2:p.Ser204Thr
ENST00000545985.5:c.830G>C ENSP00000475241.2:p.Ser277Thr
NM_001164277.1:c.830G>C , LRG_187t1:c.830G>C NP_001157749.1:p.Ser277Thr
NM_001164278.1:c.830G>C NP_001157750.1:p.Ser277Thr
NM_001164279.1:c.611G>C NP_001157751.1:p.Ser204Thr
NM_001164280.1:c.830G>C NP_001157752.1:p.Ser277Thr
NM_001467.5:c.830G>C NP_001458.1:p.Ser277Thr
NM_001164278.2:c.830G>C NP_001157750.1:p.Ser277Thr
NM_001164279.2:c.611G>C NP_001157751.1:p.Ser204Thr
NM_001164280.2:c.830G>C NP_001157752.1:p.Ser277Thr
NM_001467.6:c.830G>C NP_001458.1:p.Ser277Thr
NM_001164277.2:c.830G>C MANE Select NP_001157749.1:p.Ser277Thr