Canonical Allele Identifier: CA477367870

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898525G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027815G>A , CM000673.2:g.119027815G>A	GRCh38
NC_000011.9:g.118898525G>A , CM000673.1:g.118898525G>A	GRCh37
NC_000011.8:g.118403735G>A	NCBI36
NG_013331.1:g.8092C>T , LRG_187:g.8092C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.668C>T
ENST00000697845.1:n.592C>T
ENST00000697846.1:n.668C>T
ENST00000697847.1:n.668C>T
ENST00000697848.1:n.668C>T
ENST00000697849.1:n.1707C>T
ENST00000697850.1:n.668C>T
ENST00000697851.1:n.2028C>T
ENST00000638186.1:n.742C>T
ENST00000638360.1:n.619-45C>T
ENST00000638925.1:n.675C>T
ENST00000650539.1:n.844C>T
ENST00000330775.9:c.439C>T	ENSP00000476242.2:p.Leu147=
ENST00000357590.9:c.439C>T	ENSP00000476176.2:p.Leu147=
ENST00000524428.5:n.760C>T
ENST00000525039.5:n.862C>T
ENST00000525102.5:n.1196C>T
ENST00000525372.5:n.439C>T
ENST00000525787.1:n.1055C>T
ENST00000526275.5:n.1220C>T
ENST00000526626.6:n.401C>T
ENST00000527992.5:n.666C>T
ENST00000529510.5:n.399+379C>T
ENST00000530407.5:n.588C>T
ENST00000532085.1:n.3049C>T
ENST00000532888.6:n.734C>T
ENST00000538950.5:c.220C>T	ENSP00000475991.2:p.Leu74=
ENST00000545985.5:c.439C>T	ENSP00000475241.2:p.Leu147=
NM_001164277.1:c.439C>T , LRG_187t1:c.439C>T	NP_001157749.1:p.Leu147=
NM_001164278.1:c.439C>T	NP_001157750.1:p.Leu147=
NM_001164279.1:c.220C>T	NP_001157751.1:p.Leu74=
NM_001164280.1:c.439C>T	NP_001157752.1:p.Leu147=
NM_001467.5:c.439C>T	NP_001458.1:p.Leu147=
NM_001164278.2:c.439C>T	NP_001157750.1:p.Leu147=
NM_001164279.2:c.220C>T	NP_001157751.1:p.Leu74=
NM_001164280.2:c.439C>T	NP_001157752.1:p.Leu147=
NM_001467.6:c.439C>T	NP_001458.1:p.Leu147=
NM_001164277.2:c.439C>T MANE Select	NP_001157749.1:p.Leu147=