Canonical Allele Identifier: CA382897848

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896745A>T (hg19) ; chr11:g.119026035A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026035A>T , CM000673.2:g.119026035A>T	GRCh38
NC_000011.9:g.118896745A>T , CM000673.1:g.118896745A>T	GRCh37
NC_000011.8:g.118401955A>T	NCBI36
NG_013331.1:g.9871T>A , LRG_187:g.9871T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1060T>A
ENST00000697845.1:n.1840T>A
ENST00000697846.1:n.1060T>A
ENST00000697847.1:n.1202-278T>A
ENST00000697848.1:n.1146T>A
ENST00000697849.1:n.2955T>A
ENST00000697850.1:n.1146T>A
ENST00000697851.1:n.2754T>A
ENST00000638186.1:n.1220T>A
ENST00000638360.1:n.1052T>A
ENST00000638925.1:n.1185T>A
ENST00000650539.1:n.1322T>A
ENST00000330775.9:c.916T>A	ENSP00000476242.2:p.Phe306Ile
ENST00000357590.9:c.916T>A	ENSP00000476176.2:p.Phe306Ile
ENST00000524428.5:n.1152T>A
ENST00000525039.5:n.1340T>A
ENST00000525102.5:n.1674T>A
ENST00000525372.5:n.1014T>A
ENST00000526275.5:n.1698T>A
ENST00000527992.5:n.1144T>A
ENST00000529510.5:n.604T>A
ENST00000530407.5:n.1066T>A
ENST00000532085.1:n.4297T>A
ENST00000538950.5:c.697T>A	ENSP00000475991.2:p.Phe233Ile
ENST00000545985.5:c.916T>A	ENSP00000475241.2:p.Phe306Ile
NM_001164277.1:c.916T>A , LRG_187t1:c.916T>A	NP_001157749.1:p.Phe306Ile
NM_001164278.1:c.916T>A	NP_001157750.1:p.Phe306Ile
NM_001164279.1:c.697T>A	NP_001157751.1:p.Phe233Ile
NM_001164280.1:c.916T>A	NP_001157752.1:p.Phe306Ile
NM_001467.5:c.916T>A	NP_001458.1:p.Phe306Ile
NM_001164278.2:c.916T>A	NP_001157750.1:p.Phe306Ile
NM_001164279.2:c.697T>A	NP_001157751.1:p.Phe233Ile
NM_001164280.2:c.916T>A	NP_001157752.1:p.Phe306Ile
NM_001467.6:c.916T>A	NP_001458.1:p.Phe306Ile
NM_001164277.2:c.916T>A MANE Select	NP_001157749.1:p.Phe306Ile