Canonical Allele Identifier: CA477125299

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897340G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026630G>C , CM000673.2:g.119026630G>C	GRCh38
NC_000011.9:g.118897340G>C , CM000673.1:g.118897340G>C	GRCh37
NC_000011.8:g.118402550G>C	NCBI36
NG_013331.1:g.9276C>G , LRG_187:g.9276C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+307C>G
ENST00000697845.1:n.1245C>G
ENST00000697846.1:n.1014+307C>G
ENST00000697847.1:n.1073C>G
ENST00000697848.1:n.1073C>G
ENST00000697849.1:n.2360C>G
ENST00000697850.1:n.1073C>G
ENST00000697851.1:n.2681C>G
ENST00000638186.1:n.1147C>G
ENST00000638360.1:n.979C>G
ENST00000638925.1:n.1080C>G
ENST00000650539.1:n.1249C>G
ENST00000330775.9:c.843C>G	ENSP00000476242.2:p.Gly281=
ENST00000357590.9:c.843C>G	ENSP00000476176.2:p.Gly281=
ENST00000524428.5:n.1106+307C>G
ENST00000525039.5:n.1267C>G
ENST00000525102.5:n.1601C>G
ENST00000525372.5:n.844C>G
ENST00000526275.5:n.1625C>G
ENST00000527992.5:n.1071C>G
ENST00000529510.5:n.558+307C>G
ENST00000530407.5:n.993C>G
ENST00000532085.1:n.3702C>G
ENST00000538950.5:c.624C>G	ENSP00000475991.2:p.Gly208=
ENST00000545985.5:c.843C>G	ENSP00000475241.2:p.Gly281=
NM_001164277.1:c.843C>G , LRG_187t1:c.843C>G	NP_001157749.1:p.Gly281=
NM_001164278.1:c.843C>G	NP_001157750.1:p.Gly281=
NM_001164279.1:c.624C>G	NP_001157751.1:p.Gly208=
NM_001164280.1:c.843C>G	NP_001157752.1:p.Gly281=
NM_001467.5:c.843C>G	NP_001458.1:p.Gly281=
NM_001164278.2:c.843C>G	NP_001157750.1:p.Gly281=
NM_001164279.2:c.624C>G	NP_001157751.1:p.Gly208=
NM_001164280.2:c.843C>G	NP_001157752.1:p.Gly281=
NM_001467.6:c.843C>G	NP_001458.1:p.Gly281=
NM_001164277.2:c.843C>G MANE Select	NP_001157749.1:p.Gly281=