Canonical Allele Identifier: CA477367897

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898556A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027846A>C , CM000673.2:g.119027846A>C	GRCh38
NC_000011.9:g.118898556A>C , CM000673.1:g.118898556A>C	GRCh37
NC_000011.8:g.118403766A>C	NCBI36
NG_013331.1:g.8061T>G , LRG_187:g.8061T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.637T>G
ENST00000697845.1:n.561T>G
ENST00000697846.1:n.637T>G
ENST00000697847.1:n.637T>G
ENST00000697848.1:n.637T>G
ENST00000697849.1:n.1676T>G
ENST00000697850.1:n.637T>G
ENST00000697851.1:n.1997T>G
ENST00000638186.1:n.711T>G
ENST00000638360.1:n.619-76T>G
ENST00000638925.1:n.644T>G
ENST00000650539.1:n.813T>G
ENST00000330775.9:c.408T>G	ENSP00000476242.2:p.Thr136=
ENST00000357590.9:c.408T>G	ENSP00000476176.2:p.Thr136=
ENST00000524428.5:n.729T>G
ENST00000525039.5:n.831T>G
ENST00000525102.5:n.1165T>G
ENST00000525372.5:n.408T>G
ENST00000525787.1:n.1024T>G
ENST00000526275.5:n.1189T>G
ENST00000526626.6:n.370T>G
ENST00000527992.5:n.635T>G
ENST00000529510.5:n.399+348T>G
ENST00000530407.5:n.557T>G
ENST00000532085.1:n.3018T>G
ENST00000532888.6:n.703T>G
ENST00000538950.5:c.189T>G	ENSP00000475991.2:p.Thr63=
ENST00000545985.5:c.408T>G	ENSP00000475241.2:p.Thr136=
NM_001164277.1:c.408T>G , LRG_187t1:c.408T>G	NP_001157749.1:p.Thr136=
NM_001164278.1:c.408T>G	NP_001157750.1:p.Thr136=
NM_001164279.1:c.189T>G	NP_001157751.1:p.Thr63=
NM_001164280.1:c.408T>G	NP_001157752.1:p.Thr136=
NM_001467.5:c.408T>G	NP_001458.1:p.Thr136=
NM_001164278.2:c.408T>G	NP_001157750.1:p.Thr136=
NM_001164279.2:c.189T>G	NP_001157751.1:p.Thr63=
NM_001164280.2:c.408T>G	NP_001157752.1:p.Thr136=
NM_001467.6:c.408T>G	NP_001458.1:p.Thr136=
NM_001164277.2:c.408T>G MANE Select	NP_001157749.1:p.Thr136=