Canonical Allele Identifier: CA382901282

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119027011-A-G
• MyVariant Identifiers: chr11:g.118897721A>G (hg19) ; chr11:g.119027011A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027011A>G , CM000673.2:g.119027011A>G	GRCh38
NC_000011.9:g.118897721A>G , CM000673.1:g.118897721A>G	GRCh37
NC_000011.8:g.118402931A>G	NCBI36
NG_013331.1:g.8895T>C , LRG_187:g.8895T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.940T>C
ENST00000697845.1:n.864T>C
ENST00000697846.1:n.940T>C
ENST00000697847.1:n.940T>C
ENST00000697848.1:n.940T>C
ENST00000697849.1:n.1979T>C
ENST00000697850.1:n.940T>C
ENST00000697851.1:n.2300T>C
ENST00000638186.1:n.1014T>C
ENST00000638360.1:n.846T>C
ENST00000638925.1:n.947T>C
ENST00000650539.1:n.1116T>C
ENST00000330775.9:c.710T>C	ENSP00000476242.2:p.Phe237Ser
ENST00000357590.9:c.710T>C	ENSP00000476176.2:p.Phe237Ser
ENST00000524428.5:n.1032T>C
ENST00000525039.5:n.1134T>C
ENST00000525102.5:n.1468T>C
ENST00000525372.5:n.711T>C
ENST00000526275.5:n.1492T>C
ENST00000526626.6:n.673T>C
ENST00000527992.5:n.938T>C
ENST00000529510.5:n.484T>C
ENST00000530407.5:n.860T>C
ENST00000532085.1:n.3321T>C
ENST00000532888.6:n.1006T>C
ENST00000538950.5:c.491T>C	ENSP00000475991.2:p.Phe164Ser
ENST00000545985.5:c.710T>C	ENSP00000475241.2:p.Phe237Ser
NM_001164277.1:c.710T>C , LRG_187t1:c.710T>C	NP_001157749.1:p.Phe237Ser
NM_001164278.1:c.710T>C	NP_001157750.1:p.Phe237Ser
NM_001164279.1:c.491T>C	NP_001157751.1:p.Phe164Ser
NM_001164280.1:c.710T>C	NP_001157752.1:p.Phe237Ser
NM_001467.5:c.710T>C	NP_001458.1:p.Phe237Ser
NM_001164278.2:c.710T>C	NP_001157750.1:p.Phe237Ser
NM_001164279.2:c.491T>C	NP_001157751.1:p.Phe164Ser
NM_001164280.2:c.710T>C	NP_001157752.1:p.Phe237Ser
NM_001467.6:c.710T>C	NP_001458.1:p.Phe237Ser
NM_001164277.2:c.710T>C MANE Select	NP_001157749.1:p.Phe237Ser