Canonical Allele Identifier: CA477125354

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897373T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026663T>C , CM000673.2:g.119026663T>C	GRCh38
NC_000011.9:g.118897373T>C , CM000673.1:g.118897373T>C	GRCh37
NC_000011.8:g.118402583T>C	NCBI36
NG_013331.1:g.9243A>G , LRG_187:g.9243A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+274A>G
ENST00000697845.1:n.1212A>G
ENST00000697846.1:n.1014+274A>G
ENST00000697847.1:n.1040A>G
ENST00000697848.1:n.1040A>G
ENST00000697849.1:n.2327A>G
ENST00000697850.1:n.1040A>G
ENST00000697851.1:n.2648A>G
ENST00000638186.1:n.1114A>G
ENST00000638360.1:n.946A>G
ENST00000638925.1:n.1047A>G
ENST00000650539.1:n.1216A>G
ENST00000330775.9:c.810A>G	ENSP00000476242.2:p.Glu270=
ENST00000357590.9:c.810A>G	ENSP00000476176.2:p.Glu270=
ENST00000524428.5:n.1106+274A>G
ENST00000525039.5:n.1234A>G
ENST00000525102.5:n.1568A>G
ENST00000525372.5:n.811A>G
ENST00000526275.5:n.1592A>G
ENST00000527992.5:n.1038A>G
ENST00000529510.5:n.558+274A>G
ENST00000530407.5:n.960A>G
ENST00000532085.1:n.3669A>G
ENST00000538950.5:c.591A>G	ENSP00000475991.2:p.Glu197=
ENST00000545985.5:c.810A>G	ENSP00000475241.2:p.Glu270=
NM_001164277.1:c.810A>G , LRG_187t1:c.810A>G	NP_001157749.1:p.Glu270=
NM_001164278.1:c.810A>G	NP_001157750.1:p.Glu270=
NM_001164279.1:c.591A>G	NP_001157751.1:p.Glu197=
NM_001164280.1:c.810A>G	NP_001157752.1:p.Glu270=
NM_001467.5:c.810A>G	NP_001458.1:p.Glu270=
NM_001164278.2:c.810A>G	NP_001157750.1:p.Glu270=
NM_001164279.2:c.591A>G	NP_001157751.1:p.Glu197=
NM_001164280.2:c.810A>G	NP_001157752.1:p.Glu270=
NM_001467.6:c.810A>G	NP_001458.1:p.Glu270=
NM_001164277.2:c.810A>G MANE Select	NP_001157749.1:p.Glu270=