Canonical Allele Identifier: CA2003748829

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026009G= , CM000673.2:g.119026009G=	GRCh38
NC_000011.9:g.118896719G= , CM000673.1:g.118896719G=	GRCh37
NC_000011.8:g.118401929G=	NCBI36
NG_013331.1:g.9897C= , LRG_187:g.9897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1086C=
ENST00000697845.1:n.1866C=
ENST00000697846.1:n.1086C=
ENST00000697847.1:n.1202-252C=
ENST00000697848.1:n.1172C=
ENST00000697849.1:n.2981C=
ENST00000697850.1:n.1172C=
ENST00000697851.1:n.2780C=
ENST00000638186.1:n.1246C=
ENST00000638360.1:n.1078C=
ENST00000638925.1:n.1211C=
ENST00000650539.1:n.1348C=
ENST00000330775.9:c.942C=	ENSP00000476242.2:p.Ser314=
ENST00000357590.9:c.942C=	ENSP00000476176.2:p.Ser314=
ENST00000524428.5:n.1178C=
ENST00000525039.5:n.1366C=
ENST00000525102.5:n.1700C=
ENST00000525372.5:n.1040C=
ENST00000526275.5:n.1724C=
ENST00000527992.5:n.1170C=
ENST00000529510.5:n.630C=
ENST00000530407.5:n.1092C=
ENST00000532085.1:n.4323C=
ENST00000538950.5:c.723C=	ENSP00000475991.2:p.Ser241=
ENST00000545985.5:c.942C=	ENSP00000475241.2:p.Ser314=
NM_001164277.1:c.942C= , LRG_187t1:c.942C=	NP_001157749.1:p.Ser314=
NM_001164278.1:c.942C=	NP_001157750.1:p.Ser314=
NM_001164279.1:c.723C=	NP_001157751.1:p.Ser241=
NM_001164280.1:c.942C=	NP_001157752.1:p.Ser314=
NM_001467.5:c.942C=	NP_001458.1:p.Ser314=
NM_001164278.2:c.942C=	NP_001157750.1:p.Ser314=
NM_001164279.2:c.723C=	NP_001157751.1:p.Ser241=
NM_001164280.2:c.942C=	NP_001157752.1:p.Ser314=
NM_001467.6:c.942C=	NP_001458.1:p.Ser314=
NM_001164277.2:c.942C= MANE Select	NP_001157749.1:p.Ser314=