Canonical Allele Identifier: CA477367896

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898547G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027837G>C , CM000673.2:g.119027837G>C	GRCh38
NC_000011.9:g.118898547G>C , CM000673.1:g.118898547G>C	GRCh37
NC_000011.8:g.118403757G>C	NCBI36
NG_013331.1:g.8070C>G , LRG_187:g.8070C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.646C>G
ENST00000697845.1:n.570C>G
ENST00000697846.1:n.646C>G
ENST00000697847.1:n.646C>G
ENST00000697848.1:n.646C>G
ENST00000697849.1:n.1685C>G
ENST00000697850.1:n.646C>G
ENST00000697851.1:n.2006C>G
ENST00000638186.1:n.720C>G
ENST00000638360.1:n.619-67C>G
ENST00000638925.1:n.653C>G
ENST00000650539.1:n.822C>G
ENST00000330775.9:c.417C>G	ENSP00000476242.2:p.Ala139=
ENST00000357590.9:c.417C>G	ENSP00000476176.2:p.Ala139=
ENST00000524428.5:n.738C>G
ENST00000525039.5:n.840C>G
ENST00000525102.5:n.1174C>G
ENST00000525372.5:n.417C>G
ENST00000525787.1:n.1033C>G
ENST00000526275.5:n.1198C>G
ENST00000526626.6:n.379C>G
ENST00000527992.5:n.644C>G
ENST00000529510.5:n.399+357C>G
ENST00000530407.5:n.566C>G
ENST00000532085.1:n.3027C>G
ENST00000532888.6:n.712C>G
ENST00000538950.5:c.198C>G	ENSP00000475991.2:p.Ala66=
ENST00000545985.5:c.417C>G	ENSP00000475241.2:p.Ala139=
NM_001164277.1:c.417C>G , LRG_187t1:c.417C>G	NP_001157749.1:p.Ala139=
NM_001164278.1:c.417C>G	NP_001157750.1:p.Ala139=
NM_001164279.1:c.198C>G	NP_001157751.1:p.Ala66=
NM_001164280.1:c.417C>G	NP_001157752.1:p.Ala139=
NM_001467.5:c.417C>G	NP_001458.1:p.Ala139=
NM_001164278.2:c.417C>G	NP_001157750.1:p.Ala139=
NM_001164279.2:c.198C>G	NP_001157751.1:p.Ala66=
NM_001164280.2:c.417C>G	NP_001157752.1:p.Ala139=
NM_001467.6:c.417C>G	NP_001458.1:p.Ala139=
NM_001164277.2:c.417C>G MANE Select	NP_001157749.1:p.Ala139=