Canonical Allele Identifier: CA2003748809

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025974G= , CM000673.2:g.119025974G=	GRCh38
NC_000011.9:g.118896684G= , CM000673.1:g.118896684G=	GRCh37
NC_000011.8:g.118401894G=	NCBI36
NG_013331.1:g.9932C= , LRG_187:g.9932C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1121C=
ENST00000697845.1:n.1901C=
ENST00000697846.1:n.1121C=
ENST00000697847.1:n.1202-217C=
ENST00000697848.1:n.1207C=
ENST00000697849.1:n.3016C=
ENST00000697850.1:n.1207C=
ENST00000697851.1:n.2815C=
ENST00000638186.1:n.1281C=
ENST00000638360.1:n.1113C=
ENST00000638925.1:n.1246C=
ENST00000650539.1:n.1383C=
ENST00000330775.9:c.977C=	ENSP00000476242.2:p.Ser326=
ENST00000357590.9:c.977C=	ENSP00000476176.2:p.Ser326=
ENST00000524428.5:n.1213C=
ENST00000525039.5:n.1401C=
ENST00000525102.5:n.1735C=
ENST00000525372.5:n.1075C=
ENST00000526275.5:n.1759C=
ENST00000527992.5:n.1205C=
ENST00000529510.5:n.665C=
ENST00000530407.5:n.1127C=
ENST00000532085.1:n.4358C=
ENST00000538950.5:c.758C=	ENSP00000475991.2:p.Ser253=
ENST00000545985.5:c.977C=	ENSP00000475241.2:p.Ser326=
NM_001164277.1:c.977C= , LRG_187t1:c.977C=	NP_001157749.1:p.Ser326=
NM_001164278.1:c.977C=	NP_001157750.1:p.Ser326=
NM_001164279.1:c.758C=	NP_001157751.1:p.Ser253=
NM_001164280.1:c.977C=	NP_001157752.1:p.Ser326=
NM_001467.5:c.977C=	NP_001458.1:p.Ser326=
NM_001164278.2:c.977C=	NP_001157750.1:p.Ser326=
NM_001164279.2:c.758C=	NP_001157751.1:p.Ser253=
NM_001164280.2:c.977C=	NP_001157752.1:p.Ser326=
NM_001467.6:c.977C=	NP_001458.1:p.Ser326=
NM_001164277.2:c.977C= MANE Select	NP_001157749.1:p.Ser326=