Canonical Allele Identifier: CA2003750561
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119028804C= , CM000673.2:g.119028804C= GRCh38
NC_000011.9:g.118899514C= , CM000673.1:g.118899514C= GRCh37
NC_000011.8:g.118404724C= NCBI36
NG_013331.1:g.7103G= , LRG_187:g.7103G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.378-378G=
ENST00000697846.1:n.378-378G=
ENST00000697847.1:n.378-378G=
ENST00000697848.1:n.378-378G=
ENST00000697849.1:n.1039G=
ENST00000697850.1:n.378-378G=
ENST00000697851.1:n.1039G=
ENST00000638186.1:n.452-378G=
ENST00000638360.1:n.386-378G=
ENST00000638925.1:n.385-378G=
ENST00000650539.1:n.554-378G=
ENST00000330775.9:c.149-378G= ENSP00000476242.2:n.149-378G=
ENST00000357590.9:c.149-378G= ENSP00000476176.2:n.149-378G=
ENST00000524428.5:n.149-378G=
ENST00000525039.5:n.572-378G=
ENST00000525102.5:n.906-378G=
ENST00000525372.5:n.149-378G=
ENST00000525787.1:n.444-378G=
ENST00000526275.5:n.231G=
ENST00000526626.6:n.343+418G=
ENST00000527992.5:n.376-378G=
ENST00000529510.5:n.167-378G=
ENST00000530407.5:n.228G=
ENST00000532085.1:n.2060G=
ENST00000532888.6:n.374G=
ENST00000534384.1:n.369-378G=
ENST00000538950.5:c.-141G= ENSP00000475991.2:n.-141G=
ENST00000545985.5:c.149-378G= ENSP00000475241.2:n.149-378G=
NM_001164277.1:c.149-378G= , LRG_187t1:c.149-378G= NP_001157749.1:n.149-378G=
NM_001164278.1:c.149-378G= NP_001157750.1:n.149-378G=
NM_001164279.1:c.-141G= NP_001157751.1:n.-141G=
NM_001164280.1:c.149-378G= NP_001157752.1:n.149-378G=
NM_001467.5:c.149-378G= NP_001458.1:n.149-378G=
NM_001164278.2:c.149-378G= NP_001157750.1:n.149-378G=
NM_001164279.2:c.-141G= NP_001157751.1:n.-141G=
NM_001164280.2:c.149-378G= NP_001157752.1:n.149-378G=
NM_001467.6:c.149-378G= NP_001458.1:n.149-378G=
NM_001164277.2:c.149-378G= MANE Select NP_001157749.1:n.149-378G=