Canonical Allele Identifier: CA2003749745

Gene: SLC37A4

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.683G=
ENST00000697845.1:n.607G=
ENST00000697846.1:n.683G=
ENST00000697847.1:n.683G=
ENST00000697848.1:n.683G=
ENST00000697849.1:n.1722G=
ENST00000697850.1:n.683G=
ENST00000697851.1:n.2043G=
ENST00000638186.1:n.757G=
ENST00000638360.1:n.619-30G=
ENST00000638925.1:n.690G=
ENST00000650539.1:n.859G=
ENST00000330775.9:c.454G=	ENSP00000476242.2:p.Gly152=
ENST00000357590.9:c.454G=	ENSP00000476176.2:p.Gly152=
ENST00000524428.5:n.775G=
ENST00000525039.5:n.877G=
ENST00000525102.5:n.1211G=
ENST00000525372.5:n.454G=
ENST00000526275.5:n.1235G=
ENST00000526626.6:n.416G=
ENST00000527992.5:n.681G=
ENST00000529510.5:n.399+394G=
ENST00000530407.5:n.603G=
ENST00000532085.1:n.3064G=
ENST00000532888.6:n.749G=
ENST00000538950.5:c.235G=	ENSP00000475991.2:p.Gly79=
ENST00000545985.5:c.454G=	ENSP00000475241.2:p.Gly152=
NM_001164277.1:c.454G= , LRG_187t1:c.454G=	NP_001157749.1:p.Gly152=
NM_001164278.1:c.454G=	NP_001157750.1:p.Gly152=
NM_001164279.1:c.235G=	NP_001157751.1:p.Gly79=
NM_001164280.1:c.454G=	NP_001157752.1:p.Gly152=
NM_001467.5:c.454G=	NP_001458.1:p.Gly152=
NM_001164278.2:c.454G=	NP_001157750.1:p.Gly152=
NM_001164279.2:c.235G=	NP_001157751.1:p.Gly79=
NM_001164280.2:c.454G=	NP_001157752.1:p.Gly152=
NM_001467.6:c.454G=	NP_001458.1:p.Gly152=
NM_001164277.2:c.454G= MANE Select	NP_001157749.1:p.Gly152=