Canonical Allele Identifier: CA2003749344

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027029G= , CM000673.2:g.119027029G=	GRCh38
NC_000011.9:g.118897739G= , CM000673.1:g.118897739G=	GRCh37
NC_000011.8:g.118402949G=	NCBI36
NG_013331.1:g.8877C= , LRG_187:g.8877C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.922C=
ENST00000697845.1:n.846C=
ENST00000697846.1:n.922C=
ENST00000697847.1:n.922C=
ENST00000697848.1:n.922C=
ENST00000697849.1:n.1961C=
ENST00000697850.1:n.922C=
ENST00000697851.1:n.2282C=
ENST00000638186.1:n.996C=
ENST00000638360.1:n.828C=
ENST00000638925.1:n.929C=
ENST00000650539.1:n.1098C=
ENST00000330775.9:c.692C=	ENSP00000476242.2:p.Thr231=
ENST00000357590.9:c.692C=	ENSP00000476176.2:p.Thr231=
ENST00000524428.5:n.1014C=
ENST00000525039.5:n.1116C=
ENST00000525102.5:n.1450C=
ENST00000525372.5:n.693C=
ENST00000526275.5:n.1474C=
ENST00000526626.6:n.655C=
ENST00000527992.5:n.920C=
ENST00000529510.5:n.466C=
ENST00000530407.5:n.842C=
ENST00000532085.1:n.3303C=
ENST00000532888.6:n.988C=
ENST00000538950.5:c.473C=	ENSP00000475991.2:p.Thr158=
ENST00000545985.5:c.692C=	ENSP00000475241.2:p.Thr231=
NM_001164277.1:c.692C= , LRG_187t1:c.692C=	NP_001157749.1:p.Thr231=
NM_001164278.1:c.692C=	NP_001157750.1:p.Thr231=
NM_001164279.1:c.473C=	NP_001157751.1:p.Thr158=
NM_001164280.1:c.692C=	NP_001157752.1:p.Thr231=
NM_001467.5:c.692C=	NP_001458.1:p.Thr231=
NM_001164278.2:c.692C=	NP_001157750.1:p.Thr231=
NM_001164279.2:c.473C=	NP_001157751.1:p.Thr158=
NM_001164280.2:c.692C=	NP_001157752.1:p.Thr231=
NM_001467.6:c.692C=	NP_001458.1:p.Thr231=
NM_001164277.2:c.692C= MANE Select	NP_001157749.1:p.Thr231=