Canonical Allele Identifier: CA2003749515

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027369A= , CM000673.2:g.119027369A=	GRCh38
NC_000011.9:g.118898079A= , CM000673.1:g.118898079A=	GRCh37
NC_000011.8:g.118403289A=	NCBI36
NG_013331.1:g.8537T= , LRG_187:g.8537T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.855+259T=
ENST00000697845.1:n.779+259T=
ENST00000697846.1:n.855+259T=
ENST00000697847.1:n.855+259T=
ENST00000697848.1:n.855+259T=
ENST00000697849.1:n.1894+259T=
ENST00000697850.1:n.855+259T=
ENST00000697851.1:n.2215+259T=
ENST00000638186.1:n.929+259T=
ENST00000638360.1:n.761+259T=
ENST00000638925.1:n.862+259T=
ENST00000650539.1:n.1031+259T=
ENST00000330775.9:c.625+259T=	ENSP00000476242.2:n.625+259T=
ENST00000357590.9:c.625+259T=	ENSP00000476176.2:n.625+259T=
ENST00000524428.5:n.947+259T=
ENST00000525039.5:n.1049+259T=
ENST00000525102.5:n.1383+259T=
ENST00000525372.5:n.626+259T=
ENST00000526275.5:n.1407+259T=
ENST00000526626.6:n.588+259T=
ENST00000527992.5:n.853+259T=
ENST00000529510.5:n.400-274T=
ENST00000530407.5:n.775+259T=
ENST00000532085.1:n.3236+259T=
ENST00000532888.6:n.921+259T=
ENST00000538950.5:c.406+259T=	ENSP00000475991.2:n.406+259T=
ENST00000545985.5:c.625+259T=	ENSP00000475241.2:n.625+259T=
NM_001164277.1:c.625+259T= , LRG_187t1:c.625+259T=	NP_001157749.1:n.625+259T=
NM_001164278.1:c.625+259T=	NP_001157750.1:n.625+259T=
NM_001164279.1:c.406+259T=	NP_001157751.1:n.406+259T=
NM_001164280.1:c.625+259T=	NP_001157752.1:n.625+259T=
NM_001467.5:c.625+259T=	NP_001458.1:n.625+259T=
NM_001164278.2:c.625+259T=	NP_001157750.1:n.625+259T=
NM_001164279.2:c.406+259T=	NP_001157751.1:n.406+259T=
NM_001164280.2:c.625+259T=	NP_001157752.1:n.625+259T=
NM_001467.6:c.625+259T=	NP_001458.1:n.625+259T=
NM_001164277.2:c.625+259T= MANE Select	NP_001157749.1:n.625+259T=