Canonical Allele Identifier: CA477125255

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897313C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026603C>T , CM000673.2:g.119026603C>T	GRCh38
NC_000011.9:g.118897313C>T , CM000673.1:g.118897313C>T	GRCh37
NC_000011.8:g.118402523C>T	NCBI36
NG_013331.1:g.9303G>A , LRG_187:g.9303G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+334G>A
ENST00000697845.1:n.1272G>A
ENST00000697846.1:n.1014+334G>A
ENST00000697847.1:n.1100G>A
ENST00000697848.1:n.1100G>A
ENST00000697849.1:n.2387G>A
ENST00000697850.1:n.1100G>A
ENST00000697851.1:n.2708G>A
ENST00000638186.1:n.1174G>A
ENST00000638360.1:n.1006G>A
ENST00000638925.1:n.1107G>A
ENST00000650539.1:n.1276G>A
ENST00000330775.9:c.870G>A	ENSP00000476242.2:p.Lys290=
ENST00000357590.9:c.870G>A	ENSP00000476176.2:p.Lys290=
ENST00000524428.5:n.1106+334G>A
ENST00000525039.5:n.1294G>A
ENST00000525102.5:n.1628G>A
ENST00000525372.5:n.871G>A
ENST00000526275.5:n.1652G>A
ENST00000527992.5:n.1098G>A
ENST00000529510.5:n.558+334G>A
ENST00000530407.5:n.1020G>A
ENST00000532085.1:n.3729G>A
ENST00000538950.5:c.651G>A	ENSP00000475991.2:p.Lys217=
ENST00000545985.5:c.870G>A	ENSP00000475241.2:p.Lys290=
NM_001164277.1:c.870G>A , LRG_187t1:c.870G>A	NP_001157749.1:p.Lys290=
NM_001164278.1:c.870G>A	NP_001157750.1:p.Lys290=
NM_001164279.1:c.651G>A	NP_001157751.1:p.Lys217=
NM_001164280.1:c.870G>A	NP_001157752.1:p.Lys290=
NM_001467.5:c.870G>A	NP_001458.1:p.Lys290=
NM_001164278.2:c.870G>A	NP_001157750.1:p.Lys290=
NM_001164279.2:c.651G>A	NP_001157751.1:p.Lys217=
NM_001164280.2:c.870G>A	NP_001157752.1:p.Lys290=
NM_001467.6:c.870G>A	NP_001458.1:p.Lys290=
NM_001164277.2:c.870G>A MANE Select	NP_001157749.1:p.Lys290=