Canonical Allele Identifier: CA2003749731

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027781A= , CM000673.2:g.119027781A=	GRCh38
NC_000011.9:g.118898491A= , CM000673.1:g.118898491A=	GRCh37
NC_000011.8:g.118403701A=	NCBI36
NG_013331.1:g.8126T= , LRG_187:g.8126T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.702T=
ENST00000697845.1:n.626T=
ENST00000697846.1:n.702T=
ENST00000697847.1:n.702T=
ENST00000697848.1:n.702T=
ENST00000697849.1:n.1741T=
ENST00000697850.1:n.702T=
ENST00000697851.1:n.2062T=
ENST00000638186.1:n.776T=
ENST00000638360.1:n.619-11T=
ENST00000638925.1:n.709T=
ENST00000650539.1:n.878T=
ENST00000330775.9:c.473T=	ENSP00000476242.2:p.Ile158=
ENST00000357590.9:c.473T=	ENSP00000476176.2:p.Ile158=
ENST00000524428.5:n.794T=
ENST00000525039.5:n.896T=
ENST00000525102.5:n.1230T=
ENST00000525372.5:n.473T=
ENST00000526275.5:n.1254T=
ENST00000526626.6:n.435T=
ENST00000527992.5:n.700T=
ENST00000529510.5:n.399+413T=
ENST00000530407.5:n.622T=
ENST00000532085.1:n.3083T=
ENST00000532888.6:n.768T=
ENST00000538950.5:c.254T=	ENSP00000475991.2:p.Ile85=
ENST00000545985.5:c.473T=	ENSP00000475241.2:p.Ile158=
NM_001164277.1:c.473T= , LRG_187t1:c.473T=	NP_001157749.1:p.Ile158=
NM_001164278.1:c.473T=	NP_001157750.1:p.Ile158=
NM_001164279.1:c.254T=	NP_001157751.1:p.Ile85=
NM_001164280.1:c.473T=	NP_001157752.1:p.Ile158=
NM_001467.5:c.473T=	NP_001458.1:p.Ile158=
NM_001164278.2:c.473T=	NP_001157750.1:p.Ile158=
NM_001164279.2:c.254T=	NP_001157751.1:p.Ile85=
NM_001164280.2:c.473T=	NP_001157752.1:p.Ile158=
NM_001467.6:c.473T=	NP_001458.1:p.Ile158=
NM_001164277.2:c.473T= MANE Select	NP_001157749.1:p.Ile158=