Canonical Allele Identifier: CA382901410

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897739G>C (hg19) ; chr11:g.119027029G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027029G>C , CM000673.2:g.119027029G>C	GRCh38
NC_000011.9:g.118897739G>C , CM000673.1:g.118897739G>C	GRCh37
NC_000011.8:g.118402949G>C	NCBI36
NG_013331.1:g.8877C>G , LRG_187:g.8877C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.922C>G
ENST00000697845.1:n.846C>G
ENST00000697846.1:n.922C>G
ENST00000697847.1:n.922C>G
ENST00000697848.1:n.922C>G
ENST00000697849.1:n.1961C>G
ENST00000697850.1:n.922C>G
ENST00000697851.1:n.2282C>G
ENST00000638186.1:n.996C>G
ENST00000638360.1:n.828C>G
ENST00000638925.1:n.929C>G
ENST00000650539.1:n.1098C>G
ENST00000330775.9:c.692C>G	ENSP00000476242.2:p.Thr231Ser
ENST00000357590.9:c.692C>G	ENSP00000476176.2:p.Thr231Ser
ENST00000524428.5:n.1014C>G
ENST00000525039.5:n.1116C>G
ENST00000525102.5:n.1450C>G
ENST00000525372.5:n.693C>G
ENST00000526275.5:n.1474C>G
ENST00000526626.6:n.655C>G
ENST00000527992.5:n.920C>G
ENST00000529510.5:n.466C>G
ENST00000530407.5:n.842C>G
ENST00000532085.1:n.3303C>G
ENST00000532888.6:n.988C>G
ENST00000538950.5:c.473C>G	ENSP00000475991.2:p.Thr158Ser
ENST00000545985.5:c.692C>G	ENSP00000475241.2:p.Thr231Ser
NM_001164277.1:c.692C>G , LRG_187t1:c.692C>G	NP_001157749.1:p.Thr231Ser
NM_001164278.1:c.692C>G	NP_001157750.1:p.Thr231Ser
NM_001164279.1:c.473C>G	NP_001157751.1:p.Thr158Ser
NM_001164280.1:c.692C>G	NP_001157752.1:p.Thr231Ser
NM_001467.5:c.692C>G	NP_001458.1:p.Thr231Ser
NM_001164278.2:c.692C>G	NP_001157750.1:p.Thr231Ser
NM_001164279.2:c.473C>G	NP_001157751.1:p.Thr158Ser
NM_001164280.2:c.692C>G	NP_001157752.1:p.Thr231Ser
NM_001467.6:c.692C>G	NP_001458.1:p.Thr231Ser
NM_001164277.2:c.692C>G MANE Select	NP_001157749.1:p.Thr231Ser