Canonical Allele Identifier: CA477367861

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898520A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027810A>C , CM000673.2:g.119027810A>C	GRCh38
NC_000011.9:g.118898520A>C , CM000673.1:g.118898520A>C	GRCh37
NC_000011.8:g.118403730A>C	NCBI36
NG_013331.1:g.8097T>G , LRG_187:g.8097T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.673T>G
ENST00000697845.1:n.597T>G
ENST00000697846.1:n.673T>G
ENST00000697847.1:n.673T>G
ENST00000697848.1:n.673T>G
ENST00000697849.1:n.1712T>G
ENST00000697850.1:n.673T>G
ENST00000697851.1:n.2033T>G
ENST00000638186.1:n.747T>G
ENST00000638360.1:n.619-40T>G
ENST00000638925.1:n.680T>G
ENST00000650539.1:n.849T>G
ENST00000330775.9:c.444T>G	ENSP00000476242.2:p.Ala148=
ENST00000357590.9:c.444T>G	ENSP00000476176.2:p.Ala148=
ENST00000524428.5:n.765T>G
ENST00000525039.5:n.867T>G
ENST00000525102.5:n.1201T>G
ENST00000525372.5:n.444T>G
ENST00000526275.5:n.1225T>G
ENST00000526626.6:n.406T>G
ENST00000527992.5:n.671T>G
ENST00000529510.5:n.399+384T>G
ENST00000530407.5:n.593T>G
ENST00000532085.1:n.3054T>G
ENST00000532888.6:n.739T>G
ENST00000538950.5:c.225T>G	ENSP00000475991.2:p.Ala75=
ENST00000545985.5:c.444T>G	ENSP00000475241.2:p.Ala148=
NM_001164277.1:c.444T>G , LRG_187t1:c.444T>G	NP_001157749.1:p.Ala148=
NM_001164278.1:c.444T>G	NP_001157750.1:p.Ala148=
NM_001164279.1:c.225T>G	NP_001157751.1:p.Ala75=
NM_001164280.1:c.444T>G	NP_001157752.1:p.Ala148=
NM_001467.5:c.444T>G	NP_001458.1:p.Ala148=
NM_001164278.2:c.444T>G	NP_001157750.1:p.Ala148=
NM_001164279.2:c.225T>G	NP_001157751.1:p.Ala75=
NM_001164280.2:c.444T>G	NP_001157752.1:p.Ala148=
NM_001467.6:c.444T>G	NP_001458.1:p.Ala148=
NM_001164277.2:c.444T>G MANE Select	NP_001157749.1:p.Ala148=