Canonical Allele Identifier: CA477125346

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897367C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026657C>G , CM000673.2:g.119026657C>G	GRCh38
NC_000011.9:g.118897367C>G , CM000673.1:g.118897367C>G	GRCh37
NC_000011.8:g.118402577C>G	NCBI36
NG_013331.1:g.9249G>C , LRG_187:g.9249G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+280G>C
ENST00000697845.1:n.1218G>C
ENST00000697846.1:n.1014+280G>C
ENST00000697847.1:n.1046G>C
ENST00000697848.1:n.1046G>C
ENST00000697849.1:n.2333G>C
ENST00000697850.1:n.1046G>C
ENST00000697851.1:n.2654G>C
ENST00000638186.1:n.1120G>C
ENST00000638360.1:n.952G>C
ENST00000638925.1:n.1053G>C
ENST00000650539.1:n.1222G>C
ENST00000330775.9:c.816G>C	ENSP00000476242.2:p.Gly272=
ENST00000357590.9:c.816G>C	ENSP00000476176.2:p.Gly272=
ENST00000524428.5:n.1106+280G>C
ENST00000525039.5:n.1240G>C
ENST00000525102.5:n.1574G>C
ENST00000525372.5:n.817G>C
ENST00000526275.5:n.1598G>C
ENST00000527992.5:n.1044G>C
ENST00000529510.5:n.558+280G>C
ENST00000530407.5:n.966G>C
ENST00000532085.1:n.3675G>C
ENST00000538950.5:c.597G>C	ENSP00000475991.2:p.Gly199=
ENST00000545985.5:c.816G>C	ENSP00000475241.2:p.Gly272=
NM_001164277.1:c.816G>C , LRG_187t1:c.816G>C	NP_001157749.1:p.Gly272=
NM_001164278.1:c.816G>C	NP_001157750.1:p.Gly272=
NM_001164279.1:c.597G>C	NP_001157751.1:p.Gly199=
NM_001164280.1:c.816G>C	NP_001157752.1:p.Gly272=
NM_001467.5:c.816G>C	NP_001458.1:p.Gly272=
NM_001164278.2:c.816G>C	NP_001157750.1:p.Gly272=
NM_001164279.2:c.597G>C	NP_001157751.1:p.Gly199=
NM_001164280.2:c.816G>C	NP_001157752.1:p.Gly272=
NM_001467.6:c.816G>C	NP_001458.1:p.Gly272=
NM_001164277.2:c.816G>C MANE Select	NP_001157749.1:p.Gly272=