Canonical Allele Identifier: CA2003749345

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027031G= , CM000673.2:g.119027031G=	GRCh38
NC_000011.9:g.118897741G= , CM000673.1:g.118897741G=	GRCh37
NC_000011.8:g.118402951G=	NCBI36
NG_013331.1:g.8875C= , LRG_187:g.8875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.920C=
ENST00000697845.1:n.844C=
ENST00000697846.1:n.920C=
ENST00000697847.1:n.920C=
ENST00000697848.1:n.920C=
ENST00000697849.1:n.1959C=
ENST00000697850.1:n.920C=
ENST00000697851.1:n.2280C=
ENST00000638186.1:n.994C=
ENST00000638360.1:n.826C=
ENST00000638925.1:n.927C=
ENST00000650539.1:n.1096C=
ENST00000330775.9:c.690C=	ENSP00000476242.2:p.Ser230=
ENST00000357590.9:c.690C=	ENSP00000476176.2:p.Ser230=
ENST00000524428.5:n.1012C=
ENST00000525039.5:n.1114C=
ENST00000525102.5:n.1448C=
ENST00000525372.5:n.691C=
ENST00000526275.5:n.1472C=
ENST00000526626.6:n.653C=
ENST00000527992.5:n.918C=
ENST00000529510.5:n.464C=
ENST00000530407.5:n.840C=
ENST00000532085.1:n.3301C=
ENST00000532888.6:n.986C=
ENST00000538950.5:c.471C=	ENSP00000475991.2:p.Ser157=
ENST00000545985.5:c.690C=	ENSP00000475241.2:p.Ser230=
NM_001164277.1:c.690C= , LRG_187t1:c.690C=	NP_001157749.1:p.Ser230=
NM_001164278.1:c.690C=	NP_001157750.1:p.Ser230=
NM_001164279.1:c.471C=	NP_001157751.1:p.Ser157=
NM_001164280.1:c.690C=	NP_001157752.1:p.Ser230=
NM_001467.5:c.690C=	NP_001458.1:p.Ser230=
NM_001164278.2:c.690C=	NP_001157750.1:p.Ser230=
NM_001164279.2:c.471C=	NP_001157751.1:p.Ser157=
NM_001164280.2:c.690C=	NP_001157752.1:p.Ser230=
NM_001467.6:c.690C=	NP_001458.1:p.Ser230=
NM_001164277.2:c.690C= MANE Select	NP_001157749.1:p.Ser230=