Canonical Allele Identifier: CA382903407

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943620080
• gnomAD v4: 11-119027800-C-A
• MyVariant Identifiers: chr11:g.118898510C>A (hg19) ; chr11:g.119027800C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027800C>A , CM000673.2:g.119027800C>A	GRCh38
NC_000011.9:g.118898510C>A , CM000673.1:g.118898510C>A	GRCh37
NC_000011.8:g.118403720C>A	NCBI36
NG_013331.1:g.8107G>T , LRG_187:g.8107G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.683G>T
ENST00000697845.1:n.607G>T
ENST00000697846.1:n.683G>T
ENST00000697847.1:n.683G>T
ENST00000697848.1:n.683G>T
ENST00000697849.1:n.1722G>T
ENST00000697850.1:n.683G>T
ENST00000697851.1:n.2043G>T
ENST00000638186.1:n.757G>T
ENST00000638360.1:n.619-30G>T
ENST00000638925.1:n.690G>T
ENST00000650539.1:n.859G>T
ENST00000330775.9:c.454G>T	ENSP00000476242.2:p.Gly152Cys
ENST00000357590.9:c.454G>T	ENSP00000476176.2:p.Gly152Cys
ENST00000524428.5:n.775G>T
ENST00000525039.5:n.877G>T
ENST00000525102.5:n.1211G>T
ENST00000525372.5:n.454G>T
ENST00000526275.5:n.1235G>T
ENST00000526626.6:n.416G>T
ENST00000527992.5:n.681G>T
ENST00000529510.5:n.399+394G>T
ENST00000530407.5:n.603G>T
ENST00000532085.1:n.3064G>T
ENST00000532888.6:n.749G>T
ENST00000538950.5:c.235G>T	ENSP00000475991.2:p.Gly79Cys
ENST00000545985.5:c.454G>T	ENSP00000475241.2:p.Gly152Cys
NM_001164277.1:c.454G>T , LRG_187t1:c.454G>T	NP_001157749.1:p.Gly152Cys
NM_001164278.1:c.454G>T	NP_001157750.1:p.Gly152Cys
NM_001164279.1:c.235G>T	NP_001157751.1:p.Gly79Cys
NM_001164280.1:c.454G>T	NP_001157752.1:p.Gly152Cys
NM_001467.5:c.454G>T	NP_001458.1:p.Gly152Cys
NM_001164278.2:c.454G>T	NP_001157750.1:p.Gly152Cys
NM_001164279.2:c.235G>T	NP_001157751.1:p.Gly79Cys
NM_001164280.2:c.454G>T	NP_001157752.1:p.Gly152Cys
NM_001467.6:c.454G>T	NP_001458.1:p.Gly152Cys
NM_001164277.2:c.454G>T MANE Select	NP_001157749.1:p.Gly152Cys