Canonical Allele Identifier: CA477125336
Gene: SLC37A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118897361A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119026651A>T , CM000673.2:g.119026651A>T GRCh38
NC_000011.9:g.118897361A>T , CM000673.1:g.118897361A>T GRCh37
NC_000011.8:g.118402571A>T NCBI36
NG_013331.1:g.9255T>A , LRG_187:g.9255T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1014+286T>A
ENST00000697845.1:n.1224T>A
ENST00000697846.1:n.1014+286T>A
ENST00000697847.1:n.1052T>A
ENST00000697848.1:n.1052T>A
ENST00000697849.1:n.2339T>A
ENST00000697850.1:n.1052T>A
ENST00000697851.1:n.2660T>A
ENST00000638186.1:n.1126T>A
ENST00000638360.1:n.958T>A
ENST00000638925.1:n.1059T>A
ENST00000650539.1:n.1228T>A
ENST00000330775.9:c.822T>A ENSP00000476242.2:p.Leu274=
ENST00000357590.9:c.822T>A ENSP00000476176.2:p.Leu274=
ENST00000524428.5:n.1106+286T>A
ENST00000525039.5:n.1246T>A
ENST00000525102.5:n.1580T>A
ENST00000525372.5:n.823T>A
ENST00000526275.5:n.1604T>A
ENST00000527992.5:n.1050T>A
ENST00000529510.5:n.558+286T>A
ENST00000530407.5:n.972T>A
ENST00000532085.1:n.3681T>A
ENST00000538950.5:c.603T>A ENSP00000475991.2:p.Leu201=
ENST00000545985.5:c.822T>A ENSP00000475241.2:p.Leu274=
NM_001164277.1:c.822T>A , LRG_187t1:c.822T>A NP_001157749.1:p.Leu274=
NM_001164278.1:c.822T>A NP_001157750.1:p.Leu274=
NM_001164279.1:c.603T>A NP_001157751.1:p.Leu201=
NM_001164280.1:c.822T>A NP_001157752.1:p.Leu274=
NM_001467.5:c.822T>A NP_001458.1:p.Leu274=
NM_001164278.2:c.822T>A NP_001157750.1:p.Leu274=
NM_001164279.2:c.603T>A NP_001157751.1:p.Leu201=
NM_001164280.2:c.822T>A NP_001157752.1:p.Leu274=
NM_001467.6:c.822T>A NP_001458.1:p.Leu274=
NM_001164277.2:c.822T>A MANE Select NP_001157749.1:p.Leu274=