Canonical Allele Identifier: CA477125804

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897699A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026989A>G , CM000673.2:g.119026989A>G	GRCh38
NC_000011.9:g.118897699A>G , CM000673.1:g.118897699A>G	GRCh37
NC_000011.8:g.118402909A>G	NCBI36
NG_013331.1:g.8917T>C , LRG_187:g.8917T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.962T>C
ENST00000697845.1:n.886T>C
ENST00000697846.1:n.962T>C
ENST00000697847.1:n.962T>C
ENST00000697848.1:n.962T>C
ENST00000697849.1:n.2001T>C
ENST00000697850.1:n.962T>C
ENST00000697851.1:n.2322T>C
ENST00000638186.1:n.1036T>C
ENST00000638360.1:n.868T>C
ENST00000638925.1:n.969T>C
ENST00000650539.1:n.1138T>C
ENST00000330775.9:c.732T>C	ENSP00000476242.2:p.Thr244=
ENST00000357590.9:c.732T>C	ENSP00000476176.2:p.Thr244=
ENST00000524428.5:n.1054T>C
ENST00000525039.5:n.1156T>C
ENST00000525102.5:n.1490T>C
ENST00000525372.5:n.733T>C
ENST00000526275.5:n.1514T>C
ENST00000526626.6:n.695T>C
ENST00000527992.5:n.960T>C
ENST00000529510.5:n.506T>C
ENST00000530407.5:n.882T>C
ENST00000532085.1:n.3343T>C
ENST00000532888.6:n.1028T>C
ENST00000538950.5:c.513T>C	ENSP00000475991.2:p.Thr171=
ENST00000545985.5:c.732T>C	ENSP00000475241.2:p.Thr244=
NM_001164277.1:c.732T>C , LRG_187t1:c.732T>C	NP_001157749.1:p.Thr244=
NM_001164278.1:c.732T>C	NP_001157750.1:p.Thr244=
NM_001164279.1:c.513T>C	NP_001157751.1:p.Thr171=
NM_001164280.1:c.732T>C	NP_001157752.1:p.Thr244=
NM_001467.5:c.732T>C	NP_001458.1:p.Thr244=
NM_001164278.2:c.732T>C	NP_001157750.1:p.Thr244=
NM_001164279.2:c.513T>C	NP_001157751.1:p.Thr171=
NM_001164280.2:c.732T>C	NP_001157752.1:p.Thr244=
NM_001467.6:c.732T>C	NP_001458.1:p.Thr244=
NM_001164277.2:c.732T>C MANE Select	NP_001157749.1:p.Thr244=