Canonical Allele Identifier: CA2003750575
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119028812T= , CM000673.2:g.119028812T= GRCh38
NC_000011.9:g.118899522T= , CM000673.1:g.118899522T= GRCh37
NC_000011.8:g.118404732T= NCBI36
NG_013331.1:g.7095A= , LRG_187:g.7095A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.378-386A=
ENST00000697846.1:n.378-386A=
ENST00000697847.1:n.378-386A=
ENST00000697848.1:n.378-386A=
ENST00000697849.1:n.1031A=
ENST00000697850.1:n.378-386A=
ENST00000697851.1:n.1031A=
ENST00000638186.1:n.452-386A=
ENST00000638360.1:n.386-386A=
ENST00000638925.1:n.385-386A=
ENST00000650539.1:n.554-386A=
ENST00000330775.9:c.149-386A= ENSP00000476242.2:n.149-386A=
ENST00000357590.9:c.149-386A= ENSP00000476176.2:n.149-386A=
ENST00000524428.5:n.149-386A=
ENST00000525039.5:n.572-386A=
ENST00000525102.5:n.906-386A=
ENST00000525372.5:n.149-386A=
ENST00000525787.1:n.444-386A=
ENST00000526275.5:n.223A=
ENST00000526626.6:n.343+410A=
ENST00000527992.5:n.376-386A=
ENST00000529510.5:n.167-386A=
ENST00000530407.5:n.220A=
ENST00000532085.1:n.2052A=
ENST00000532888.6:n.366A=
ENST00000534384.1:n.369-386A=
ENST00000538950.5:c.-149A= ENSP00000475991.2:n.-149A=
ENST00000545985.5:c.149-386A= ENSP00000475241.2:n.149-386A=
NM_001164277.1:c.149-386A= , LRG_187t1:c.149-386A= NP_001157749.1:n.149-386A=
NM_001164278.1:c.149-386A= NP_001157750.1:n.149-386A=
NM_001164279.1:c.-149A= NP_001157751.1:n.-149A=
NM_001164280.1:c.149-386A= NP_001157752.1:n.149-386A=
NM_001467.5:c.149-386A= NP_001458.1:n.149-386A=
NM_001164278.2:c.149-386A= NP_001157750.1:n.149-386A=
NM_001164279.2:c.-149A= NP_001157751.1:n.-149A=
NM_001164280.2:c.149-386A= NP_001157752.1:n.149-386A=
NM_001467.6:c.149-386A= NP_001458.1:n.149-386A=
NM_001164277.2:c.149-386A= MANE Select NP_001157749.1:n.149-386A=