Canonical Allele Identifier: CA477129669

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118899963C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029253C>G , CM000673.2:g.119029253C>G	GRCh38
NC_000011.9:g.118899963C>G , CM000673.1:g.118899963C>G	GRCh37
NC_000011.8:g.118405173C>G	NCBI36
NG_013331.1:g.6654G>C , LRG_187:g.6654G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.346G>C
ENST00000697846.1:n.346G>C
ENST00000697847.1:n.346G>C
ENST00000697848.1:n.346G>C
ENST00000697849.1:n.590G>C
ENST00000697850.1:n.346G>C
ENST00000697851.1:n.590G>C
ENST00000638186.1:n.420G>C
ENST00000638360.1:n.354G>C
ENST00000638925.1:n.353G>C
ENST00000650539.1:n.522G>C
ENST00000330775.9:c.117G>C	ENSP00000476242.2:p.Val39=
ENST00000357590.9:c.117G>C	ENSP00000476176.2:p.Val39=
ENST00000524428.5:n.117G>C
ENST00000525039.5:n.540G>C
ENST00000525102.5:n.874G>C
ENST00000525372.5:n.117G>C
ENST00000525787.1:n.412G>C
ENST00000526626.6:n.312G>C
ENST00000527992.5:n.344G>C
ENST00000529510.5:n.135G>C
ENST00000530407.5:n.197+139G>C
ENST00000532085.1:n.1611G>C
ENST00000532888.6:n.312G>C
ENST00000534384.1:n.337G>C
ENST00000538950.5:c.-172+139G>C	ENSP00000475991.2:n.-172+139G>C
ENST00000545985.5:c.117G>C	ENSP00000475241.2:p.Val39=
NM_001164277.1:c.117G>C , LRG_187t1:c.117G>C	NP_001157749.1:p.Val39=
NM_001164278.1:c.117G>C	NP_001157750.1:p.Val39=
NM_001164279.1:c.-172+139G>C	NP_001157751.1:n.-172+139G>C
NM_001164280.1:c.117G>C	NP_001157752.1:p.Val39=
NM_001467.5:c.117G>C	NP_001458.1:p.Val39=
NM_001164278.2:c.117G>C	NP_001157750.1:p.Val39=
NM_001164279.2:c.-172+139G>C	NP_001157751.1:n.-172+139G>C
NM_001164280.2:c.117G>C	NP_001157752.1:p.Val39=
NM_001467.6:c.117G>C	NP_001458.1:p.Val39=
NM_001164277.2:c.117G>C MANE Select	NP_001157749.1:p.Val39=