Canonical Allele Identifier: CA2003749161

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026686T= , CM000673.2:g.119026686T=	GRCh38
NC_000011.9:g.118897396T= , CM000673.1:g.118897396T=	GRCh37
NC_000011.8:g.118402606T=	NCBI36
NG_013331.1:g.9220A= , LRG_187:g.9220A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+251A=
ENST00000697845.1:n.1189A=
ENST00000697846.1:n.1014+251A=
ENST00000697847.1:n.1017A=
ENST00000697848.1:n.1017A=
ENST00000697849.1:n.2304A=
ENST00000697850.1:n.1017A=
ENST00000697851.1:n.2625A=
ENST00000638186.1:n.1091A=
ENST00000638360.1:n.923A=
ENST00000638925.1:n.1024A=
ENST00000650539.1:n.1193A=
ENST00000330775.9:c.787A=	ENSP00000476242.2:p.Ser263=
ENST00000357590.9:c.787A=	ENSP00000476176.2:p.Ser263=
ENST00000524428.5:n.1106+251A=
ENST00000525039.5:n.1211A=
ENST00000525102.5:n.1545A=
ENST00000525372.5:n.788A=
ENST00000526275.5:n.1569A=
ENST00000527992.5:n.1015A=
ENST00000529510.5:n.558+251A=
ENST00000530407.5:n.937A=
ENST00000532085.1:n.3646A=
ENST00000532888.6:n.1331A=
ENST00000538950.5:c.568A=	ENSP00000475991.2:p.Ser190=
ENST00000545985.5:c.787A=	ENSP00000475241.2:p.Ser263=
NM_001164277.1:c.787A= , LRG_187t1:c.787A=	NP_001157749.1:p.Ser263=
NM_001164278.1:c.787A=	NP_001157750.1:p.Ser263=
NM_001164279.1:c.568A=	NP_001157751.1:p.Ser190=
NM_001164280.1:c.787A=	NP_001157752.1:p.Ser263=
NM_001467.5:c.787A=	NP_001458.1:p.Ser263=
NM_001164278.2:c.787A=	NP_001157750.1:p.Ser263=
NM_001164279.2:c.568A=	NP_001157751.1:p.Ser190=
NM_001164280.2:c.787A=	NP_001157752.1:p.Ser263=
NM_001467.6:c.787A=	NP_001458.1:p.Ser263=
NM_001164277.2:c.787A= MANE Select	NP_001157749.1:p.Ser263=